Canonical Allele Identifier: CA479876892
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814226-G-A
COSMIC: COSM1212834
MyVariant Identifiers: chr12:g.53208010G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814226G>A , CM000674.2:g.52814226G>A GRCh38
NC_000012.11:g.53208010G>A , CM000674.1:g.53208010G>A GRCh37
NC_000012.10:g.51494277G>A NCBI36
NG_007380.1:g.5326C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-168C>T ENSP00000448220.1:n.-168C>T
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