Canonical Allele Identifier: CA6588923

Gene: KRT4

Linked Data

• dbSNP Id: rs199513369
• ExAC: 12:53208076 A / G
• gnomAD v2: 12-53208076-A-G
• gnomAD v3: 12-52814292-A-G
• gnomAD v4: 12-52814292-A-G
• MyVariant Identifiers: chr12:g.53208076A>G (hg19) ; chr12:g.52814292A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814292A>G , CM000674.2:g.52814292A>G	GRCh38
NC_000012.11:g.53208076A>G , CM000674.1:g.53208076A>G	GRCh37
NC_000012.10:g.51494343A>G	NCBI36
NG_007380.1:g.5260T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-234T>C	ENSP00000448220.1:n.-234T>C