Canonical Allele Identifier: CA379106799

Gene: TNNI2

Linked Data

• dbSNP Id: rs1847180141
• MyVariant Identifiers: chr11:g.1862685G>A (hg19) ; chr11:g.1841455G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841455G>A , CM000673.2:g.1841455G>A	GRCh38
NC_000011.9:g.1862685G>A , CM000673.1:g.1862685G>A	GRCh37
NC_000011.8:g.1819261G>A	NCBI36
NG_011621.1:g.7453G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.454-1G>A MANE Select	ENSP00000371336.1:n.454-1G>A
ENST00000252898.11:c.454-1G>A	ENSP00000252898.7:n.454-1G>A
ENST00000381905.3:c.454-1G>A	ENSP00000371330.3:n.454-1G>A
ENST00000381906.5:c.454-1G>A	ENSP00000371331.1:n.454-1G>A
ENST00000381911.5:c.454-1G>A	ENSP00000371336.1:n.454-1G>A
ENST00000617947.4:c.454-1G>A	ENSP00000481242.1:n.454-1G>A
NM_001145829.1:c.454-1G>A	NP_001139301.1:n.454-1G>A
NM_001145841.1:c.454-1G>A	NP_001139313.1:n.454-1G>A
NM_003282.3:c.454-1G>A	NP_003273.1:n.454-1G>A
NM_003282.4:c.454-1G>A MANE Select	NP_003273.1:n.454-1G>A
NM_001145829.2:c.454-1G>A	NP_001139301.1:n.454-1G>A
NM_001145841.2:c.454-1G>A	NP_001139313.1:n.454-1G>A