Canonical Allele Identifier: CA308399668
Gene: PCAT19 HGNC NCBI
MyVariant.info:
GRCh38 chr19:g.41479716T>C
gnomAD v3:
19:41479716 T / C
gnomAD v4:
chr19-41479716-T-C
Joint Max Group AF 0.49347943 (AFR)
Genomes Max Group AF 0.49347943 (AFR)
dbSNP:
887391
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_040109.1:n.950-432A>G
NR_040109.2:n.955-432A>G
NR_136334.1:n.67-432A>G
Search 100 bp 5'
Search 100 bp 3'