Canonical Allele Identifier: CA337618890
Gene:
MyVariant.info:
GRCh38 chrY:g.8399854G>A
GRCh37 chrY:g.8267895G>A
gnomAD v3:
Y:8399854 G / A
gnomAD v4:
chrY-8399854-G-A
Joint Max Group AF 0.04088547 (AFR)
Genomes Max Group AF 0.04088547 (AFR)
dbSNP:
9785694
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8399854G>A , CM000686.2:g.8399854G>A GRCh38
NC_000024.9:g.8267895G>A , CM000686.1:g.8267895G>A GRCh37
NC_000024.8:g.8327895G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938646.1:n.87-2873G>A
XR_938647.1:n.87-2873G>A
Search 100 bp 5'
Search 100 bp 3'