Canonical Allele Identifier: CA1947878810

Gene: TNNI2

Linked Data

• dbSNP Id: rs1847183536
• gnomAD v4: 11-1841555-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841555A>T , CM000673.2:g.1841555A>T	GRCh38
NC_000011.9:g.1862785A>T , CM000673.1:g.1862785A>T	GRCh37
NC_000011.8:g.1819361A>T	NCBI36
NG_011621.1:g.7553A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.*4A>T MANE Select	ENSP00000371336.1:n.*4A>T
ENST00000252898.11:c.553A>T	ENSP00000252898.7:n.553A>T
ENST00000381905.3:c.*4A>T	ENSP00000371330.3:n.*4A>T
ENST00000381906.5:c.*4A>T	ENSP00000371331.1:n.*4A>T
ENST00000381911.5:c.*4A>T	ENSP00000371336.1:n.*4A>T
ENST00000617947.4:c.*4A>T	ENSP00000481242.1:n.*4A>T
NM_001145829.1:c.*4A>T	NP_001139301.1:n.*4A>T
NM_001145841.1:c.*4A>T	NP_001139313.1:n.*4A>T
NM_003282.3:c.*4A>T	NP_003273.1:n.*4A>T
NM_003282.4:c.*4A>T MANE Select	NP_003273.1:n.*4A>T
NM_001145829.2:c.*4A>T	NP_001139301.1:n.*4A>T
NM_001145841.2:c.*4A>T	NP_001139313.1:n.*4A>T