Canonical Allele Identifier: CA471993016

Gene: TNNI2

Linked Data

• MyVariant Identifiers: chr11:g.1862700A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841470A>G , CM000673.2:g.1841470A>G	GRCh38
NC_000011.9:g.1862700A>G , CM000673.1:g.1862700A>G	GRCh37
NC_000011.8:g.1819276A>G	NCBI36
NG_011621.1:g.7468A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.468A>G MANE Select	ENSP00000371336.1:p.Arg156=
ENST00000252898.11:c.468A>G	ENSP00000252898.7:p.Arg156=
ENST00000381905.3:c.468A>G	ENSP00000371330.3:p.Arg156=
ENST00000381906.5:c.468A>G	ENSP00000371331.1:p.Arg156=
ENST00000381911.5:c.468A>G	ENSP00000371336.1:p.Arg156=
ENST00000617947.4:c.468A>G	ENSP00000481242.1:p.Arg156=
NM_001145829.1:c.468A>G	NP_001139301.1:p.Arg156=
NM_001145841.1:c.468A>G	NP_001139313.1:p.Arg156=
NM_003282.3:c.468A>G	NP_003273.1:p.Arg156=
NM_003282.4:c.468A>G MANE Select	NP_003273.1:p.Arg156=
NM_001145829.2:c.468A>G	NP_001139301.1:p.Arg156=
NM_001145841.2:c.468A>G	NP_001139313.1:p.Arg156=