Canonical Allele Identifier: CA882338254
Gene: PCAT19 HGNC NCBI

Linked Data

dbSNP Id: rs1330021507
MyVariant Identifiers: chr19:g.41479706T>C (hg38)

Genomic Alleles

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

Transcript Alleles

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