Canonical Allele Identifier: CA1866594467
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Linked Data

dbSNP Id: rs1829160818

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700046G>C , CM000671.2:g.97700046G>C GRCh38
NC_000009.11:g.100462328G>C , CM000671.1:g.100462328G>C GRCh37
NC_000009.10:g.99502149G>C NCBI36
NG_011642.1:g.2364C>G , LRG_471:g.2364C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.663-61G>C (KRT18P13)
NR_147055.1:n.1526C>G (PTCSC2)