Canonical Allele Identifier: CA585055055
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1390381082

Genomic Alleles

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

Transcript Alleles

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