Canonical Allele Identifier: CA2611933128

Gene: TNNI2

Linked Data

• gnomAD v4: 11-1841401-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.1841401A>C , CM000673.2:g.1841401A>C	GRCh38
NC_000011.9:g.1862631A>C , CM000673.1:g.1862631A>C	GRCh37
NC_000011.8:g.1819207A>C	NCBI36
NG_011621.1:g.7399A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381911.6:c.454-55A>C MANE Select	ENSP00000371336.1:n.454-55A>C
ENST00000252898.11:c.454-55A>C	ENSP00000252898.7:n.454-55A>C
ENST00000381905.3:c.454-55A>C	ENSP00000371330.3:n.454-55A>C
ENST00000381906.5:c.454-55A>C	ENSP00000371331.1:n.454-55A>C
ENST00000381911.5:c.454-55A>C	ENSP00000371336.1:n.454-55A>C
ENST00000617947.4:c.454-55A>C	ENSP00000481242.1:n.454-55A>C
NM_001145829.1:c.454-55A>C	NP_001139301.1:n.454-55A>C
NM_001145841.1:c.454-55A>C	NP_001139313.1:n.454-55A>C
NM_003282.3:c.454-55A>C	NP_003273.1:n.454-55A>C
NM_003282.4:c.454-55A>C MANE Select	NP_003273.1:n.454-55A>C
NM_001145829.2:c.454-55A>C	NP_001139301.1:n.454-55A>C
NM_001145841.2:c.454-55A>C	NP_001139313.1:n.454-55A>C