Canonical Allele Identifier: CA6588916

Gene: KRT4

Linked Data

• dbSNP Id: rs759297931
• ExAC: 12:53208023 G / A
• gnomAD v2: 12-53208023-G-A
• gnomAD v3: 12-52814239-G-A
• gnomAD v4: 12-52814239-G-A
• MyVariant Identifiers: chr12:g.53208023G>A (hg19) ; chr12:g.52814239G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814239G>A , CM000674.2:g.52814239G>A	GRCh38
NC_000012.11:g.53208023G>A , CM000674.1:g.53208023G>A	GRCh37
NC_000012.10:g.51494290G>A	NCBI36
NG_007380.1:g.5313C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-181C>T	ENSP00000448220.1:n.-181C>T