Canonical Allele Identifier: CA6588922

Gene: KRT4

Linked Data

• dbSNP Id: rs201811845
• ExAC: 12:53208046 A / G
• gnomAD v2: 12-53208046-A-G
• gnomAD v4: 12-52814262-A-G
• MyVariant Identifiers: chr12:g.53208046A>G (hg19) ; chr12:g.52814262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814262A>G , CM000674.2:g.52814262A>G	GRCh38
NC_000012.11:g.53208046A>G , CM000674.1:g.53208046A>G	GRCh37
NC_000012.10:g.51494313A>G	NCBI36
NG_007380.1:g.5290T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-204T>C	ENSP00000448220.1:n.-204T>C