Canonical Allele Identifier: CA2336487509
Gene: PCAT19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41479706T= , CM000681.2:g.41479706T= GRCh38
NC_000019.8:g.46677454T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040109.1:n.950-422A=
NR_040109.2:n.955-422A=
NR_136334.1:n.67-422A=