Canonical Allele Identifier: CA2336487499
Gene: PCAT19 HGNC NCBI

Linked Data

dbSNP Id: rs2040502813

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41479684T>A , CM000681.2:g.41479684T>A GRCh38
NC_000019.8:g.46677432T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040109.1:n.950-400A>T
NR_040109.2:n.955-400A>T
NR_136334.1:n.67-400A>T