Canonical Allele Identifier: CA216206438

Gene: TNNI2

Linked Data

• dbSNP Id: rs555004172
• gnomAD v3: 11-1841626-T-C
• gnomAD v4: 11-1841626-T-C
• MyVariant Identifiers: chr11:g.1862856T>C (hg19) ; chr11:g.1841626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841626T>C , CM000673.2:g.1841626T>C	GRCh38
NC_000011.9:g.1862856T>C , CM000673.1:g.1862856T>C	GRCh37
NC_000011.8:g.1819432T>C	NCBI36
NG_011621.1:g.7624T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*75T>C MANE Select	ENSP00000371336.1:n.*75T>C
ENST00000252898.11:c.624T>C	ENSP00000252898.7:n.624T>C
ENST00000381905.3:c.*75T>C	ENSP00000371330.3:n.*75T>C
ENST00000381906.5:c.*75T>C	ENSP00000371331.1:n.*75T>C
ENST00000381911.5:c.*75T>C	ENSP00000371336.1:n.*75T>C
ENST00000617947.4:c.*75T>C	ENSP00000481242.1:n.*75T>C
NM_001145829.1:c.*75T>C	NP_001139301.1:n.*75T>C
NM_001145841.1:c.*75T>C	NP_001139313.1:n.*75T>C
NM_003282.3:c.*75T>C	NP_003273.1:n.*75T>C
NM_003282.4:c.*75T>C MANE Select	NP_003273.1:n.*75T>C
NM_001145829.2:c.*75T>C	NP_001139301.1:n.*75T>C
NM_001145841.2:c.*75T>C	NP_001139313.1:n.*75T>C