Canonical Allele Identifier: CA379106844

Gene: TNNI2

Linked Data

• gnomAD v4: 11-1841478-G-C
• MyVariant Identifiers: chr11:g.1862708G>C (hg19) ; chr11:g.1841478G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841478G>C , CM000673.2:g.1841478G>C	GRCh38
NC_000011.9:g.1862708G>C , CM000673.1:g.1862708G>C	GRCh37
NC_000011.8:g.1819284G>C	NCBI36
NG_011621.1:g.7476G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.476G>C MANE Select	ENSP00000371336.1:p.Gly159Ala
ENST00000252898.11:c.476G>C	ENSP00000252898.7:p.Gly159Ala
ENST00000381905.3:c.476G>C	ENSP00000371330.3:p.Gly159Ala
ENST00000381906.5:c.476G>C	ENSP00000371331.1:p.Gly159Ala
ENST00000381911.5:c.476G>C	ENSP00000371336.1:p.Gly159Ala
ENST00000617947.4:c.476G>C	ENSP00000481242.1:p.Gly159Ala
NM_001145829.1:c.476G>C	NP_001139301.1:p.Gly159Ala
NM_001145841.1:c.476G>C	NP_001139313.1:p.Gly159Ala
NM_003282.3:c.476G>C	NP_003273.1:p.Gly159Ala
NM_003282.4:c.476G>C MANE Select	NP_003273.1:p.Gly159Ala
NM_001145829.2:c.476G>C	NP_001139301.1:p.Gly159Ala
NM_001145841.2:c.476G>C	NP_001139313.1:p.Gly159Ala