Canonical Allele Identifier: CA379105164
Gene: TNNI2 HGNC NCBI

Linked Data

gnomAD v4: 11-1840547-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1840547C>A , CM000673.2:g.1840547C>A GRCh38
NC_000011.9:g.1861777C>A , CM000673.1:g.1861777C>A GRCh37
NC_000011.8:g.1818353C>A NCBI36
NG_011621.1:g.6545C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000381911.6:c.77C>A MANE Select ENSP00000371336.1:p.Ala26Glu
ENST00000252898.11:c.77C>A ENSP00000252898.7:p.Ala26Glu
ENST00000381905.3:c.77C>A ENSP00000371330.3:p.Ala26Glu
ENST00000381906.5:c.77C>A ENSP00000371331.1:p.Ala26Glu
ENST00000381911.5:c.77C>A ENSP00000371336.1:p.Ala26Glu
ENST00000468473.1:n.247C>A
ENST00000617947.4:c.77C>A ENSP00000481242.1:p.Ala26Glu
NM_001145829.1:c.77C>A NP_001139301.1:p.Ala26Glu
NM_001145841.1:c.77C>A NP_001139313.1:p.Ala26Glu
NM_003282.3:c.77C>A NP_003273.1:p.Ala26Glu
NM_003282.4:c.77C>A MANE Select NP_003273.1:p.Ala26Glu
NM_001145829.2:c.77C>A NP_001139301.1:p.Ala26Glu
NM_001145841.2:c.77C>A NP_001139313.1:p.Ala26Glu