Canonical Allele Identifier: CA2618968436

Gene: KRT4

Linked Data

• dbSNP Id: rs2121258985
• gnomAD v4: 12-52814426-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814426A>G , CM000674.2:g.52814426A>G	GRCh38
NC_000012.11:g.53208210A>G , CM000674.1:g.53208210A>G	GRCh37
NC_000012.10:g.51494477A>G	NCBI36
NG_007380.1:g.5126T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-368T>C	ENSP00000448220.1:n.-368T>C