Canonical Allele Identifier: CA1866594662
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700127T= , CM000671.2:g.97700127T= GRCh38
NC_000009.11:g.100462409T= , CM000671.1:g.100462409T= GRCh37
NC_000009.10:g.99502230T= NCBI36
NG_011642.1:g.2283A= , LRG_471:g.2283A=

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.683T= (KRT18P13)
NR_147055.1:n.1501-56A= (PTCSC2)