Canonical Allele Identifier: CA479876896
Gene: KRT4 HGNC NCBI

Linked Data

COSMIC: COSM431364
MyVariant Identifiers: chr12:g.53208015T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814231T>C , CM000674.2:g.52814231T>C GRCh38
NC_000012.11:g.53208015T>C , CM000674.1:g.53208015T>C GRCh37
NC_000012.10:g.51494282T>C NCBI36
NG_007380.1:g.5321A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-173A>G ENSP00000448220.1:n.-173A>G