Canonical Allele Identifier: CA585055057
Gene: PCAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1450859095
gnomAD v2: 8-128092086-A-T
gnomAD v3: 8-127079841-A-T
gnomAD v4: 8-127079841-A-T
MyVariant Identifiers: chr8:g.128092086A>T (hg19) chr8:g.127079841A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127079841A>T , CM000670.2:g.127079841A>T GRCh38
NC_000008.10:g.128092086A>T , CM000670.1:g.128092086A>T GRCh37
NC_000008.9:g.128161268A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119373.1:n.102-708T>A
Search 100 bp 5'
Search 100 bp 3'