Canonical Allele Identifier: CA1866594469
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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