Canonical Allele Identifier: CA2596638919

Gene: KRT5

Linked Data

• dbSNP Id: rs2120492154
• gnomAD v3: 12-52520413-C-T
• gnomAD v4: 12-52520413-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520413C>T , CM000674.2:g.52520413C>T	GRCh38
NC_000012.11:g.52914197C>T , CM000674.1:g.52914197C>T	GRCh37
NC_000012.10:g.51200464C>T	NCBI36
NG_008297.1:g.5047G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.8:c.-117G>A	ENSP00000252242.4:n.-117G>A
ENST00000546577.1:c.-29G>A	ENSP00000449651.1:n.-29G>A
NM_000424.3:c.-117G>A	NP_000415.2:n.-117G>A