Canonical Allele Identifier: CA2611933317

Gene: TNNI2

Linked Data

• gnomAD v4: 11-1841624-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841624C>T , CM000673.2:g.1841624C>T	GRCh38
NC_000011.9:g.1862854C>T , CM000673.1:g.1862854C>T	GRCh37
NC_000011.8:g.1819430C>T	NCBI36
NG_011621.1:g.7622C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*73C>T MANE Select	ENSP00000371336.1:n.*73C>T
ENST00000252898.11:c.622C>T	ENSP00000252898.7:n.622C>T
ENST00000381905.3:c.*73C>T	ENSP00000371330.3:n.*73C>T
ENST00000381906.5:c.*73C>T	ENSP00000371331.1:n.*73C>T
ENST00000381911.5:c.*73C>T	ENSP00000371336.1:n.*73C>T
ENST00000617947.4:c.*73C>T	ENSP00000481242.1:n.*73C>T
NM_001145829.1:c.*73C>T	NP_001139301.1:n.*73C>T
NM_001145841.1:c.*73C>T	NP_001139313.1:n.*73C>T
NM_003282.3:c.*73C>T	NP_003273.1:n.*73C>T
NM_003282.4:c.*73C>T MANE Select	NP_003273.1:n.*73C>T
NM_001145829.2:c.*73C>T	NP_001139301.1:n.*73C>T
NM_001145841.2:c.*73C>T	NP_001139313.1:n.*73C>T