Canonical Allele Identifier: CA384945772
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs1329013108

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652051C>G , CM000674.2:g.52652051C>G GRCh38
NC_000012.11:g.53045835C>G , CM000674.1:g.53045835C>G GRCh37
NC_000012.10:g.51332102C>G NCBI36
NG_008296.1:g.5125G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.92G>C MANE Select ENSP00000310861.3:p.Gly31Ala
ENST00000309680.3:c.92G>C ENSP00000310861.3:p.Gly31Ala
NM_000423.2:c.92G>C NP_000414.2:p.Gly31Ala
NM_000423.3:c.92G>C MANE Select NP_000414.2:p.Gly31Ala