Canonical Allele Identifier: CA6585946
Gene: KRT2 HGNC NCBI

Linked Data

dbSNP Id: rs142748186

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52651984G>A , CM000674.2:g.52651984G>A GRCh38
NC_000012.11:g.53045768G>A , CM000674.1:g.53045768G>A GRCh37
NC_000012.10:g.51332035G>A NCBI36
NG_008296.1:g.5192C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.159C>T MANE Select ENSP00000310861.3:p.Phe53=
ENST00000309680.3:c.159C>T ENSP00000310861.3:p.Phe53=
NM_000423.2:c.159C>T NP_000414.2:p.Phe53=
NM_000423.3:c.159C>T MANE Select NP_000414.2:p.Phe53=