Canonical Allele Identifier: CA605088159

Gene: KRT4

Linked Data

• dbSNP Id: rs1398931641
• gnomAD v2: 12-53208110-G-A
• gnomAD v4: 12-52814326-G-A
• MyVariant Identifiers: chr12:g.53208110G>A (hg19) ; chr12:g.52814326G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814326G>A , CM000674.2:g.52814326G>A	GRCh38
NC_000012.11:g.53208110G>A , CM000674.1:g.53208110G>A	GRCh37
NC_000012.10:g.51494377G>A	NCBI36
NG_007380.1:g.5226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-268C>T	ENSP00000448220.1:n.-268C>T