Canonical Allele Identifier: CA2336487517

Gene: PCAT19

Linked Data

• dbSNP Id: rs987585408

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41479720G>T , CM000681.2:g.41479720G>T	GRCh38
NC_000019.8:g.46677468G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_040109.1:n.950-436C>A
NR_040109.2:n.955-436C>A
NR_136334.1:n.67-436C>A