Canonical Allele Identifier: CA379106969

Gene: TNNI2

Linked Data

• MyVariant Identifiers: chr11:g.1862761A>G (hg19) ; chr11:g.1841531A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841531A>G , CM000673.2:g.1841531A>G	GRCh38
NC_000011.9:g.1862761A>G , CM000673.1:g.1862761A>G	GRCh37
NC_000011.8:g.1819337A>G	NCBI36
NG_011621.1:g.7529A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.529A>G MANE Select	ENSP00000371336.1:p.Met177Val
ENST00000252898.11:c.529A>G	ENSP00000252898.7:p.Met177Val
ENST00000381905.3:c.529A>G	ENSP00000371330.3:p.Met177Val
ENST00000381906.5:c.529A>G	ENSP00000371331.1:p.Met177Val
ENST00000381911.5:c.529A>G	ENSP00000371336.1:p.Met177Val
ENST00000617947.4:c.529A>G	ENSP00000481242.1:p.Met177Val
NM_001145829.1:c.529A>G	NP_001139301.1:p.Met177Val
NM_001145841.1:c.529A>G	NP_001139313.1:p.Met177Val
NM_003282.3:c.529A>G	NP_003273.1:p.Met177Val
NM_003282.4:c.529A>G MANE Select	NP_003273.1:p.Met177Val
NM_001145829.2:c.529A>G	NP_001139301.1:p.Met177Val
NM_001145841.2:c.529A>G	NP_001139313.1:p.Met177Val