Canonical Allele Identifier: CA1818224952
Gene: PCAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079872A= , CM000670.2:g.127079872A= GRCh38
NC_000008.10:g.128092117A= , CM000670.1:g.128092117A= GRCh37
NC_000008.9:g.128161299A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-739T=