Canonical Allele Identifier: CA379106829

Gene: TNNI2

Linked Data

• dbSNP Id: rs1847180824
• gnomAD v3: 11-1841471-G-A
• gnomAD v4: 11-1841471-G-A
• MyVariant Identifiers: chr11:g.1862701G>A (hg19) ; chr11:g.1841471G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841471G>A , CM000673.2:g.1841471G>A	GRCh38
NC_000011.9:g.1862701G>A , CM000673.1:g.1862701G>A	GRCh37
NC_000011.8:g.1819277G>A	NCBI36
NG_011621.1:g.7469G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000381911.6:c.469G>A MANE Select	ENSP00000371336.1:p.Asp157Asn
ENST00000252898.11:c.469G>A	ENSP00000252898.7:p.Asp157Asn
ENST00000381905.3:c.469G>A	ENSP00000371330.3:p.Asp157Asn
ENST00000381906.5:c.469G>A	ENSP00000371331.1:p.Asp157Asn
ENST00000381911.5:c.469G>A	ENSP00000371336.1:p.Asp157Asn
ENST00000617947.4:c.469G>A	ENSP00000481242.1:p.Asp157Asn
NM_001145829.1:c.469G>A	NP_001139301.1:p.Asp157Asn
NM_001145841.1:c.469G>A	NP_001139313.1:p.Asp157Asn
NM_003282.3:c.469G>A	NP_003273.1:p.Asp157Asn
NM_003282.4:c.469G>A MANE Select	NP_003273.1:p.Asp157Asn
NM_001145829.2:c.469G>A	NP_001139301.1:p.Asp157Asn
NM_001145841.2:c.469G>A	NP_001139313.1:p.Asp157Asn