Canonical Allele Identifier: CA2690903643

Gene: KRT18P13 PTCSC2

Linked Data

• gnomAD v4: 9-97700047-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97700047A>T , CM000671.2:g.97700047A>T	GRCh38
NC_000009.11:g.100462329A>T , CM000671.1:g.100462329A>T	GRCh37
NC_000009.10:g.99502150A>T	NCBI36
NG_011642.1:g.2363T>A , LRG_471:g.2363T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000400056.3:n.663-60A>T (KRT18P13)
NR_147055.1:n.1525T>A (PTCSC2)