Canonical Allele Identifier: CA237229731

Gene: KRT5

Linked Data

• dbSNP Id: rs566090157
• gnomAD v3: 12-52520417-T-C
• gnomAD v4: 12-52520417-T-C
• MyVariant Identifiers: chr12:g.52914201T>C (hg19) ; chr12:g.52520417T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520417T>C , CM000674.2:g.52520417T>C	GRCh38
NC_000012.11:g.52914201T>C , CM000674.1:g.52914201T>C	GRCh37
NC_000012.10:g.51200468T>C	NCBI36
NG_008297.1:g.5043A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.8:c.-121A>G	ENSP00000252242.4:n.-121A>G
ENST00000546577.1:c.-33A>G	ENSP00000449651.1:n.-33A>G
NM_000424.3:c.-121A>G	NP_000415.2:n.-121A>G