Canonical Allele Identifier: CA6588912

Gene: KRT4

Linked Data

• dbSNP Id: rs377539678
• ExAC: 12:53208007 C / T
• gnomAD v2: 12-53208007-C-T
• gnomAD v4: 12-52814223-C-T
• MyVariant Identifiers: chr12:g.53208007C>T (hg19) ; chr12:g.52814223C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814223C>T , CM000674.2:g.52814223C>T	GRCh38
NC_000012.11:g.53208007C>T , CM000674.1:g.53208007C>T	GRCh37
NC_000012.10:g.51494274C>T	NCBI36
NG_007380.1:g.5329G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-165G>A	ENSP00000448220.1:n.-165G>A