Canonical Allele Identifier: CA1818224949
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813579124

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079866A>G , CM000670.2:g.127079866A>G GRCh38
NC_000008.10:g.128092111A>G , CM000670.1:g.128092111A>G GRCh37
NC_000008.9:g.128161293A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-733T>C