Canonical Allele Identifier: CA6588904

Gene: KRT4

Linked Data

• dbSNP Id: rs769991907
• ExAC: 12:53207956 C / A
• gnomAD v2: 12-53207956-C-A
• gnomAD v3: 12-52814172-C-A
• gnomAD v4: 12-52814172-C-A
• MyVariant Identifiers: chr12:g.53207956C>A (hg19) ; chr12:g.52814172C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814172C>A , CM000674.2:g.52814172C>A	GRCh38
NC_000012.11:g.53207956C>A , CM000674.1:g.53207956C>A	GRCh37
NC_000012.10:g.51494223C>A	NCBI36
NG_007380.1:g.5380G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-114G>T	ENSP00000448220.1:n.-114G>T