Canonical Allele Identifier: CA2618968367
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52814392-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814392C>A , CM000674.2:g.52814392C>A GRCh38
NC_000012.11:g.53208176C>A , CM000674.1:g.53208176C>A GRCh37
NC_000012.10:g.51494443C>A NCBI36
NG_007380.1:g.5160G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.1:c.-334G>T ENSP00000448220.1:n.-334G>T
Search 100 bp 5'
Search 100 bp 3'