Canonical Allele Identifier: CA237279174

Gene: KRT4

Linked Data

• dbSNP Id: rs555460530
• gnomAD v3: 12-52814398-C-G
• gnomAD v4: 12-52814398-C-G
• MyVariant Identifiers: chr12:g.53208182C>G (hg19) ; chr12:g.52814398C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814398C>G , CM000674.2:g.52814398C>G	GRCh38
NC_000012.11:g.53208182C>G , CM000674.1:g.53208182C>G	GRCh37
NC_000012.10:g.51494449C>G	NCBI36
NG_007380.1:g.5154G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-340G>C	ENSP00000448220.1:n.-340G>C