Canonical Allele Identifier: CA2559886520
Gene: PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079850C>T , CM000670.2:g.127079850C>T GRCh38
NC_000008.10:g.128092095C>T , CM000670.1:g.128092095C>T GRCh37
NC_000008.9:g.128161277C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-717G>A