Canonical Allele Identifier: CA379106922

Gene: TNNI2

Linked Data

• MyVariant Identifiers: chr11:g.1862740G>T (hg19) ; chr11:g.1841510G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841510G>T , CM000673.2:g.1841510G>T	GRCh38
NC_000011.9:g.1862740G>T , CM000673.1:g.1862740G>T	GRCh37
NC_000011.8:g.1819316G>T	NCBI36
NG_011621.1:g.7508G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.508G>T MANE Select	ENSP00000371336.1:p.Gly170Cys
ENST00000252898.11:c.508G>T	ENSP00000252898.7:p.Gly170Cys
ENST00000381905.3:c.508G>T	ENSP00000371330.3:p.Gly170Cys
ENST00000381906.5:c.508G>T	ENSP00000371331.1:p.Gly170Cys
ENST00000381911.5:c.508G>T	ENSP00000371336.1:p.Gly170Cys
ENST00000617947.4:c.508G>T	ENSP00000481242.1:p.Gly170Cys
NM_001145829.1:c.508G>T	NP_001139301.1:p.Gly170Cys
NM_001145841.1:c.508G>T	NP_001139313.1:p.Gly170Cys
NM_003282.3:c.508G>T	NP_003273.1:p.Gly170Cys
NM_003282.4:c.508G>T MANE Select	NP_003273.1:p.Gly170Cys
NM_001145829.2:c.508G>T	NP_001139301.1:p.Gly170Cys
NM_001145841.2:c.508G>T	NP_001139313.1:p.Gly170Cys