Canonical Allele Identifier: CA379106984
Gene: TNNI2 HGNC NCBI

Linked Data

gnomAD v4: 11-1841537-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1841537G>A , CM000673.2:g.1841537G>A GRCh38
NC_000011.9:g.1862767G>A , CM000673.1:g.1862767G>A GRCh37
NC_000011.8:g.1819343G>A NCBI36
NG_011621.1:g.7535G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000381911.6:c.535G>A MANE Select ENSP00000371336.1:p.Glu179Lys
ENST00000252898.11:c.535G>A ENSP00000252898.7:p.Glu179Lys
ENST00000381905.3:c.535G>A ENSP00000371330.3:p.Glu179Lys
ENST00000381906.5:c.535G>A ENSP00000371331.1:p.Glu179Lys
ENST00000381911.5:c.535G>A ENSP00000371336.1:p.Glu179Lys
ENST00000617947.4:c.535G>A ENSP00000481242.1:p.Glu179Lys
NM_001145829.1:c.535G>A NP_001139301.1:p.Glu179Lys
NM_001145841.1:c.535G>A NP_001139313.1:p.Glu179Lys
NM_003282.3:c.535G>A NP_003273.1:p.Glu179Lys
NM_003282.4:c.535G>A MANE Select NP_003273.1:p.Glu179Lys
NM_001145829.2:c.535G>A NP_001139301.1:p.Glu179Lys
NM_001145841.2:c.535G>A NP_001139313.1:p.Glu179Lys