Canonical Allele Identifier: CA384946715
Gene: KRT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652139T>G , CM000674.2:g.52652139T>G GRCh38
NC_000012.11:g.53045923T>G , CM000674.1:g.53045923T>G GRCh37
NC_000012.10:g.51332190T>G NCBI36
NG_008296.1:g.5037A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.4A>C MANE Select ENSP00000310861.3:p.Ser2Arg
ENST00000309680.3:c.4A>C ENSP00000310861.3:p.Ser2Arg
NM_000423.2:c.4A>C NP_000414.2:p.Ser2Arg
NM_000423.3:c.4A>C MANE Select NP_000414.2:p.Ser2Arg