Canonical Allele Identifier: CA1818224932
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1813579009
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079849dup , CM000670.2:g.127079849dup GRCh38
NC_000008.10:g.128092094dup , CM000670.1:g.128092094dup GRCh37
NC_000008.9:g.128161276dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-716dup
Search 100 bp 5'
Search 100 bp 3'