Canonical Allele Identifier: CA605088156

Gene: KRT4

Linked Data

• dbSNP Id: rs1217511324
• gnomAD v2: 12-53208057-G-T
• gnomAD v4: 12-52814273-G-T
• MyVariant Identifiers: chr12:g.53208057G>T (hg19) ; chr12:g.52814273G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52814273G>T , CM000674.2:g.52814273G>T	GRCh38
NC_000012.11:g.53208057G>T , CM000674.1:g.53208057G>T	GRCh37
NC_000012.10:g.51494324G>T	NCBI36
NG_007380.1:g.5279C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000551956.1:c.-215C>A	ENSP00000448220.1:n.-215C>A