Canonical Allele Identifier: CA947716469

Gene: KRT4

Linked Data

• dbSNP Id: rs1939971025
• gnomAD v3: 12-52814392-C-T
• gnomAD v4: 12-52814392-C-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-334G>A	ENSP00000448220.1:n.-334G>A