Canonical Allele Identifier: CA466186163

Gene: KRT18P13 PTCSC2

Linked Data

• gnomAD v4: 9-97700134-C-G
• MyVariant Identifiers: chr9:g.100462416C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97700134C>G , CM000671.2:g.97700134C>G	GRCh38
NC_000009.11:g.100462416C>G , CM000671.1:g.100462416C>G	GRCh37
NC_000009.10:g.99502237C>G	NCBI36
NG_011642.1:g.2276G>C , LRG_471:g.2276G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400056.3:n.690C>G (KRT18P13)
NR_147055.1:n.1501-63G>C (PTCSC2)