Canonical Allele Identifier: CA2690903635
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

gnomAD v4: 9-97700042-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700042A>C , CM000671.2:g.97700042A>C GRCh38
NC_000009.11:g.100462324A>C , CM000671.1:g.100462324A>C GRCh37
NC_000009.10:g.99502145A>C NCBI36
NG_011642.1:g.2368T>G , LRG_471:g.2368T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.663-65A>C (KRT18P13)
NR_147055.1:n.1530T>G (PTCSC2)