Canonical Allele Identifier: CA2560794364
Gene: PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079840G>T , CM000670.2:g.127079840G>T GRCh38
NC_000008.10:g.128092085G>T , CM000670.1:g.128092085G>T GRCh37
NC_000008.9:g.128161267G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-707C>A