Canonical Allele Identifier: CA237279159

Gene: KRT4

Linked Data

• dbSNP Id: rs900635042
• gnomAD v4: 12-52814364-C-G
• MyVariant Identifiers: chr12:g.52814364C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814364C>G , CM000674.2:g.52814364C>G	GRCh38
NC_000012.11:g.53208148C>G , CM000674.1:g.53208148C>G	GRCh37
NC_000012.10:g.51494415C>G	NCBI36
NG_007380.1:g.5188G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-306G>C	ENSP00000448220.1:n.-306G>C