Canonical Allele Identifier: CA5815325

Gene: TNNI2

Linked Data

• dbSNP Id: rs199691669
• ExAC: 11:1862800 G / A
• gnomAD v2: 11-1862800-G-A
• gnomAD v3: 11-1841570-G-A
• gnomAD v4: 11-1841570-G-A
• MyVariant Identifiers: chr11:g.1862800G>A (hg19) ; chr11:g.1841570G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841570G>A , CM000673.2:g.1841570G>A	GRCh38
NC_000011.9:g.1862800G>A , CM000673.1:g.1862800G>A	GRCh37
NC_000011.8:g.1819376G>A	NCBI36
NG_011621.1:g.7568G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*19G>A MANE Select	ENSP00000371336.1:n.*19G>A
ENST00000252898.11:c.568G>A	ENSP00000252898.7:n.568G>A
ENST00000381905.3:c.*19G>A	ENSP00000371330.3:n.*19G>A
ENST00000381906.5:c.*19G>A	ENSP00000371331.1:n.*19G>A
ENST00000381911.5:c.*19G>A	ENSP00000371336.1:n.*19G>A
ENST00000617947.4:c.*19G>A	ENSP00000481242.1:n.*19G>A
NM_001145829.1:c.*19G>A	NP_001139301.1:n.*19G>A
NM_001145841.1:c.*19G>A	NP_001139313.1:n.*19G>A
NM_003282.3:c.*19G>A	NP_003273.1:n.*19G>A
NM_003282.4:c.*19G>A MANE Select	NP_003273.1:n.*19G>A
NM_001145829.2:c.*19G>A	NP_001139301.1:n.*19G>A
NM_001145841.2:c.*19G>A	NP_001139313.1:n.*19G>A