Canonical Allele Identifier: CA2649785719

Gene: TNNT2

Linked Data

• gnomAD v4: 1-201359008-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201359008T>C , CM000663.2:g.201359008T>C	GRCh38
NC_000001.10:g.201328136T>C , CM000663.1:g.201328136T>C	GRCh37
NC_000001.9:g.199594759T>C	NCBI36
NG_007556.1:g.23670A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000455702.7:c.*202A>G	ENSP00000402238.3:n.*202A>G
ENST00000660295.1:c.*202A>G	ENSP00000499418.1:n.*202A>G
ENST00000662159.1:c.*458A>G	ENSP00000499796.1:n.*458A>G
ENST00000367318.9:c.*202A>G	ENSP00000356287.5:n.*202A>G
ENST00000367322.5:c.*202A>G	ENSP00000356291.1:n.*202A>G
ENST00000460780.5:n.2218A>G
ENST00000476888.5:n.516A>G
ENST00000491504.5:n.2308A>G
NM_000364.3:c.*202A>G	NP_000355.2:n.*202A>G
NM_001001430.2:c.*202A>G	NP_001001430.1:n.*202A>G
NM_001001431.2:c.*202A>G	NP_001001431.1:n.*202A>G
NM_001001432.2:c.*202A>G	NP_001001432.1:n.*202A>G
NM_001276345.1:c.*202A>G	NP_001263274.1:n.*202A>G
NM_001276346.1:c.*202A>G	NP_001263275.1:n.*202A>G
NM_001276347.1:c.*202A>G	NP_001263276.1:n.*202A>G