Canonical Allele Identifier: CA2690903642
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

gnomAD v4: 9-97700047-A-C

Genomic Alleles

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

Transcript Alleles

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