Canonical Allele Identifier: CA689835559

Gene: KRT5

Linked Data

• dbSNP Id: rs1167846218
• gnomAD v3: 12-52520411-G-A
• gnomAD v4: 12-52520411-G-A
• MyVariant Identifiers: chr12:g.52914195G>A (hg19) ; chr12:g.52520411G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520411G>A , CM000674.2:g.52520411G>A	GRCh38
NC_000012.11:g.52914195G>A , CM000674.1:g.52914195G>A	GRCh37
NC_000012.10:g.51200462G>A	NCBI36
NG_008297.1:g.5049C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.8:c.-115C>T	ENSP00000252242.4:n.-115C>T
ENST00000546577.1:c.-27C>T	ENSP00000449651.1:n.-27C>T
NM_000424.3:c.-115C>T	NP_000415.2:n.-115C>T