Canonical Allele Identifier: CA2336487514
Community Standard Title: NC_000019.10:g.41479716T>A
Gene: PCAT19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41479716T>A , CM000681.2:g.41479716T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
NR_040109.1:n.950-432A>T
NR_040109.2:n.955-432A>T
NR_136334.1:n.67-432A>T