Canonical Allele Identifier: CA6588913

Gene: KRT4

Linked Data

• dbSNP Id: rs760967753
• ExAC: 12:53208013 C / T
• gnomAD v2: 12-53208013-C-T
• gnomAD v4: 12-52814229-C-T
• MyVariant Identifiers: chr12:g.53208013C>T (hg19) ; chr12:g.52814229C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814229C>T , CM000674.2:g.52814229C>T	GRCh38
NC_000012.11:g.53208013C>T , CM000674.1:g.53208013C>T	GRCh37
NC_000012.10:g.51494280C>T	NCBI36
NG_007380.1:g.5323G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-171G>A	ENSP00000448220.1:n.-171G>A