Canonical Allele Identifier: CA4903615
Gene: PSCA HGNC NCBI
MyVariant.info:
GRCh38 chr8:g.142682272G>A
GRCh37 chr8:g.143763690G>A
gnomAD v2:
8:143763690 G / A
gnomAD v3:
8:142682272 G / A
gnomAD v4:
chr8-142682272-G-A
Joint Max Group AF 0.53371779 (AMR)
Genomes Max Group AF 0.5029526 (AMR)
Exomes Max Group AF 0.5441827 (AMR)
dbSNP:
10216533
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.142682272G>A , CM000670.2:g.142682272G>A GRCh38
NC_000008.10:g.143763690G>A , CM000670.1:g.143763690G>A GRCh37
NC_000008.9:g.143760692G>A NCBI36
NG_011722.2:g.6816G>A
NG_011722.3:g.16965G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301258.5:c.*140G>A MANE Select ENSP00000301258.4:n.*140G>A
ENST00000301258.4:c.*140G>A ENSP00000301258.4:n.*140G>A
ENST00000510969.1:n.708G>A
NM_005672.4:c.*140G>A NP_005663.2:n.*140G>A
NR_033343.1:n.721G>A
NM_005672.5:c.*140G>A MANE Select NP_005663.2:n.*140G>A
NR_033343.2:n.732G>A
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