Canonical Allele Identifier: CA479876869
Gene: KRT4 HGNC NCBI

Linked Data

COSMIC: COSM468553
MyVariant Identifiers: chr12:g.53207945G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814161G>T , CM000674.2:g.52814161G>T GRCh38
NC_000012.11:g.53207945G>T , CM000674.1:g.53207945G>T GRCh37
NC_000012.10:g.51494212G>T NCBI36
NG_007380.1:g.5391C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-103C>A ENSP00000448220.1:n.-103C>A