Canonical Allele Identifier: CA344204044
Gene: TNNT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 426997
ClinVar RCV Id: RCV000490178
dbSNP Id: rs1085307889
MyVariant Identifiers: chr1:g.201331151C>T (hg19) chr1:g.201362023C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.201362023C>T , CM000663.2:g.201362023C>T GRCh38
NC_000001.10:g.201331151C>T , CM000663.1:g.201331151C>T GRCh37
NC_000001.9:g.199597774C>T NCBI36
NG_007556.1:g.20655G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000455702.7:c.595-1G>A ENSP00000402238.3:n.595-1G>A
ENST00000367318.10:c.580-1G>A ENSP00000356287.5:n.580-1G>A
ENST00000367322.6:c.568-1G>A ENSP00000356291.2:n.568-1G>A
ENST00000412633.3:c.571-1G>A ENSP00000408731.2:n.571-1G>A
ENST00000422165.6:c.601-1G>A ENSP00000395163.2:n.601-1G>A
ENST00000438742.6:c.559-1G>A ENSP00000414036.2:n.559-1G>A
ENST00000455702.6:c.595-1G>A ENSP00000402238.2:n.595-1G>A
ENST00000651504.1:n.1071-1G>A
ENST00000656932.1:c.610-1G>A MANE Select ENSP00000499593.1:n.610-1G>A
ENST00000658476.1:c.580-1G>A ENSP00000499741.1:n.580-1G>A
ENST00000660295.1:c.580-1G>A ENSP00000499418.1:n.580-1G>A
ENST00000662159.1:c.163-24G>A ENSP00000499796.1:n.163-24G>A
ENST00000663843.1:c.*510-1G>A ENSP00000499590.1:n.*510-1G>A
ENST00000666449.1:c.580-1G>A ENSP00000499667.1:n.580-1G>A
ENST00000236918.11:c.610-1G>A ENSP00000236918.8:n.610-1G>A
ENST00000360372.8:c.481-1G>A ENSP00000353535.5:n.481-1G>A
ENST00000367315.6:c.588G>A ENSP00000356284.3:p.Gln196=
ENST00000367317.8:c.562-1G>A ENSP00000356286.5:n.562-1G>A
ENST00000367318.9:c.580-1G>A ENSP00000356287.5:n.580-1G>A
ENST00000367320.6:c.481-1G>A ENSP00000356289.2:n.481-1G>A
ENST00000367322.5:c.571-1G>A ENSP00000356291.1:n.571-1G>A
ENST00000421663.6:c.394-1G>A ENSP00000404134.3:n.394-1G>A
ENST00000438742.5:c.562-1G>A ENSP00000414036.1:n.562-1G>A
ENST00000458432.6:c.394-1G>A ENSP00000387874.3:n.394-1G>A
ENST00000460780.5:n.903-1G>A
ENST00000476888.5:n.65-1G>A
ENST00000491504.5:n.1819-1G>A
ENST00000509001.5:c.580-1G>A ENSP00000422031.1:n.580-1G>A
ENST00000515042.5:n.506-1G>A
NM_000364.3:c.601-1G>A NP_000355.2:n.601-1G>A
NM_001001430.2:c.580-1G>A NP_001001430.1:n.580-1G>A
NM_001001431.2:c.571-1G>A NP_001001431.1:n.571-1G>A
NM_001001432.2:c.562-1G>A NP_001001432.1:n.562-1G>A
NM_001276345.1:c.610-1G>A NP_001263274.1:n.610-1G>A
NM_001276346.1:c.481-1G>A NP_001263275.1:n.481-1G>A
NM_001276347.1:c.580-1G>A NP_001263276.1:n.580-1G>A
XM_006711508.2:c.580-1G>A XP_006711571.1:n.580-1G>A
XM_006711509.2:c.577-1G>A XP_006711572.1:n.577-1G>A
XM_011509938.1:c.610-1G>A XP_011508240.1:n.610-1G>A
XM_011509939.1:c.607-1G>A XP_011508241.1:n.607-1G>A
XM_011509940.1:c.607-1G>A XP_011508242.1:n.607-1G>A
XM_011509941.1:c.604-1G>A XP_011508243.1:n.604-1G>A
XM_011509942.1:c.565-1G>A XP_011508244.1:n.565-1G>A
XM_011509943.1:c.565-1G>A XP_011508245.1:n.565-1G>A
XM_011509944.1:c.562-1G>A XP_011508246.1:n.562-1G>A
XM_011509946.1:c.403-1G>A XP_011508248.1:n.403-1G>A
XM_006711508.3:c.580-1G>A XP_006711571.1:n.580-1G>A
XM_006711509.3:c.577-1G>A XP_006711572.1:n.577-1G>A
XM_011509938.2:c.610-1G>A XP_011508240.1:n.610-1G>A
XM_011509940.2:c.607-1G>A XP_011508242.1:n.607-1G>A
XM_011509941.2:c.604-1G>A XP_011508243.1:n.604-1G>A
XM_011509942.2:c.565-1G>A XP_011508244.1:n.565-1G>A
XM_011509943.2:c.565-1G>A XP_011508245.1:n.565-1G>A
XM_011509944.2:c.562-1G>A XP_011508246.1:n.562-1G>A
XM_017002216.2:c.577-1G>A XP_016857705.1:n.577-1G>A
XM_017002217.1:c.571-1G>A XP_016857706.1:n.571-1G>A
XM_024449450.1:c.610-1G>A XP_024305218.1:n.610-1G>A
XM_024449454.1:c.577-1G>A XP_024305222.1:n.577-1G>A
XM_024449455.1:c.577-1G>A XP_024305223.1:n.577-1G>A
NM_000364.4:c.601-1G>A NP_000355.2:n.601-1G>A
NM_001001430.3:c.580-1G>A NP_001001430.1:n.580-1G>A
NM_001001431.3:c.571-1G>A NP_001001431.1:n.571-1G>A
NM_001001432.3:c.562-1G>A NP_001001432.1:n.562-1G>A
NM_001276345.2:c.610-1G>A MANE Select NP_001263274.1:n.610-1G>A
NM_001276346.2:c.481-1G>A NP_001263275.1:n.481-1G>A
NM_001276347.2:c.580-1G>A NP_001263276.1:n.580-1G>A
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