Canonical Allele Identifier: CA337646546
Gene: RBMY2QP HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.10013848G>T
GRCh37 chrY:g.9851457G>T
gnomAD v3:
Y:10013848 G / T
gnomAD v4:
chrY-10013848-G-T
Joint Max Group AF 0.66832993 (AFR)
Genomes Max Group AF 0.66832993 (AFR)
dbSNP:
9786489
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.10013848G>T , CM000686.2:g.10013848G>T GRCh38
NC_000024.9:g.9851457G>T , CM000686.1:g.9851457G>T GRCh37
NC_000024.8:g.10461457G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000651645.1:n.834+9347C>A
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