Canonical Allele Identifier: CA2618968442

Gene: KRT4

Linked Data

• dbSNP Id: rs2121258988
• gnomAD v4: 12-52814429-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814429A>C , CM000674.2:g.52814429A>C	GRCh38
NC_000012.11:g.53208213A>C , CM000674.1:g.53208213A>C	GRCh37
NC_000012.10:g.51494480A>C	NCBI36
NG_007380.1:g.5123T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-371T>G	ENSP00000448220.1:n.-371T>G