Canonical Allele Identifier: CA120295
Gene: KRT2 HGNC NCBI

Linked Data

ClinVar Variation Id: 9314
dbSNP Id: rs56829062

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52646783C>T , CM000674.2:g.52646783C>T GRCh38
NC_000012.11:g.53040567C>T , CM000674.1:g.53040567C>T GRCh37
NC_000012.10:g.51326834C>T NCBI36
NG_008296.1:g.10393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.1426G>A MANE Select ENSP00000310861.3:p.Glu476Lys
ENST00000309680.3:c.1426G>A ENSP00000310861.3:p.Glu476Lys
NM_000423.2:c.1426G>A NP_000414.2:p.Glu476Lys
NM_000423.3:c.1426G>A MANE Select NP_000414.2:p.Glu476Lys