Canonical Allele Identifier: CA12780236
Gene: PSCA HGNC NCBI
JRK HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.142670446G>A
GRCh37 chr8:g.143751864G>A
gnomAD v2:
8:143751864 G / A
gnomAD v3:
8:142670446 G / A
gnomAD v4:
chr8-142670446-G-A
Joint Max Group AF 0.48412378 (AFR)
Genomes Max Group AF 0.48412215 (AFR)
Exomes Max Group AF 0.27090044 (NFE)
dbSNP:
2978974
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142670446G>A , CM000670.2:g.142670446G>A GRCh38
NC_000008.10:g.143751864G>A , CM000670.1:g.143751864G>A GRCh37
NC_000008.9:g.143748866G>A NCBI36
NG_012215.2:g.4538C>T
NG_011722.3:g.5139G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000505305.1:n.139G>A (PSCA)
ENST00000510969.1:n.126G>A (PSCA)
ENST00000591357.5:n.265-314C>T (JRK)
NR_033343.1:n.139G>A (PSCA)
NR_033343.2:n.150G>A (PSCA)
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