Canonical Allele Identifier: CA528089791

Gene: TNNT2

Linked Data

• dbSNP Id: rs1421422873
• gnomAD v2: 1-201328140-A-G
• gnomAD v3: 1-201359012-A-G
• gnomAD v4: 1-201359012-A-G
• MyVariant Identifiers: chr1:g.201328140A>G (hg19) ; chr1:g.201359012A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359012A>G , CM000663.2:g.201359012A>G	GRCh38
NC_000001.10:g.201328140A>G , CM000663.1:g.201328140A>G	GRCh37
NC_000001.9:g.199594763A>G	NCBI36
NG_007556.1:g.23666T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*198T>C	ENSP00000402238.3:n.*198T>C
ENST00000660295.1:c.*198T>C	ENSP00000499418.1:n.*198T>C
ENST00000662159.1:c.*454T>C	ENSP00000499796.1:n.*454T>C
ENST00000236918.11:c.1095T>C	ENSP00000236918.8:n.1095T>C
ENST00000360372.8:c.966T>C	ENSP00000353535.5:n.966T>C
ENST00000367317.8:c.1047T>C	ENSP00000356286.5:n.1047T>C
ENST00000367318.9:c.*198T>C	ENSP00000356287.5:n.*198T>C
ENST00000367322.5:c.*198T>C	ENSP00000356291.1:n.*198T>C
ENST00000458432.6:c.*198T>C	ENSP00000387874.3:n.*198T>C
ENST00000460780.5:n.2214T>C
ENST00000476888.5:n.512T>C
ENST00000491504.5:n.2304T>C
NM_000364.3:c.*198T>C	NP_000355.2:n.*198T>C
NM_001001430.2:c.*198T>C	NP_001001430.1:n.*198T>C
NM_001001431.2:c.*198T>C	NP_001001431.1:n.*198T>C
NM_001001432.2:c.*198T>C	NP_001001432.1:n.*198T>C
NM_001276345.1:c.*198T>C	NP_001263274.1:n.*198T>C
NM_001276346.1:c.*198T>C	NP_001263275.1:n.*198T>C
NM_001276347.1:c.*198T>C	NP_001263276.1:n.*198T>C