Canonical Allele Identifier: CA1866594458
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829160742
gnomAD v4: 9-97700043-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700043A>G , CM000671.2:g.97700043A>G GRCh38
NC_000009.11:g.100462325A>G , CM000671.1:g.100462325A>G GRCh37
NC_000009.10:g.99502146A>G NCBI36
NG_011642.1:g.2367T>C , LRG_471:g.2367T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.663-64A>G (KRT18P13)
NR_147055.1:n.1529T>C (PTCSC2)