Canonical Allele Identifier: CA2336487523
Gene: PCAT19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41479731G= , CM000681.2:g.41479731G= GRCh38
NC_000019.8:g.46677479G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_040109.1:n.950-447C=
NR_040109.2:n.955-447C=
NR_136334.1:n.67-447C=