Canonical Allele Identifier: CA1818224931
Gene: PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079848A= , CM000670.2:g.127079848A= GRCh38
NC_000008.10:g.128092093A= , CM000670.1:g.128092093A= GRCh37
NC_000008.9:g.128161275A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-715T=