Canonical Allele Identifier: CA384946606
Gene: KRT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652132T>A , CM000674.2:g.52652132T>A GRCh38
NC_000012.11:g.53045916T>A , CM000674.1:g.53045916T>A GRCh37
NC_000012.10:g.51332183T>A NCBI36
NG_008296.1:g.5044A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.11A>T MANE Select ENSP00000310861.3:p.Gln4Leu
ENST00000309680.3:c.11A>T ENSP00000310861.3:p.Gln4Leu
NM_000423.2:c.11A>T NP_000414.2:p.Gln4Leu
NM_000423.3:c.11A>T MANE Select NP_000414.2:p.Gln4Leu