Canonical Allele Identifier: CA337639409
Gene: RBMY3AP HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.9610745A>G
GRCh37 chrY:g.9448354A>G
gnomAD v3:
Y:9610745 A / G
gnomAD v4:
chrY-9610745-A-G
Joint Max Group AF 0.12002326 (MID)
Genomes Max Group AF 0.05001288 (AMR)
Exomes Max Group AF 0.09179764 (MID)
dbSNP:
35567891
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.9610745A>G , CM000686.2:g.9610745A>G GRCh38
NC_000024.9:g.9448354A>G , CM000686.1:g.9448354A>G GRCh37
NC_000024.8:g.10058354A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000449381.1:n.971T>C
NR_001573.1:n.293T>C
NR_001573.2:n.293T>C
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