Canonical Allele Identifier: CA466186151

Gene: KRT18P13 PTCSC2

Linked Data

• gnomAD v4: 9-97700132-A-G
• MyVariant Identifiers: chr9:g.100462414A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97700132A>G , CM000671.2:g.97700132A>G	GRCh38
NC_000009.11:g.100462414A>G , CM000671.1:g.100462414A>G	GRCh37
NC_000009.10:g.99502235A>G	NCBI36
NG_011642.1:g.2278T>C , LRG_471:g.2278T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400056.3:n.688A>G (KRT18P13)
NR_147055.1:n.1501-61T>C (PTCSC2)