Canonical Allele Identifier: CA1866594461
Gene: KRT18P13 HGNC NCBI
PTCSC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97700045G= , CM000671.2:g.97700045G= GRCh38
NC_000009.11:g.100462327G= , CM000671.1:g.100462327G= GRCh37
NC_000009.10:g.99502148G= NCBI36
NG_011642.1:g.2365C= , LRG_471:g.2365C=

Transcript Alleles

HGVS Amino-acid change
ENST00000400056.3:n.663-62G= (KRT18P13)
NR_147055.1:n.1527C= (PTCSC2)