Canonical Allele Identifier: CA479876907
Gene: KRT4 HGNC NCBI

Linked Data

COSMIC: COSM317536
MyVariant Identifiers: chr12:g.53208028C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814244C>A , CM000674.2:g.52814244C>A GRCh38
NC_000012.11:g.53208028C>A , CM000674.1:g.53208028C>A GRCh37
NC_000012.10:g.51494295C>A NCBI36
NG_007380.1:g.5308G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-186G>T ENSP00000448220.1:n.-186G>T