Canonical Allele Identifier: CA337441109
Gene: HSFY3P HGNC NCBI
RPS4Y1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.2885045G>A
GRCh37 chrY:g.2753086G>A
gnomAD v3:
Y:2885045 G / A
gnomAD v4:
chrY-2885045-G-A
Joint Max Group AF 0.00066616 (AFR)
Genomes Max Group AF 0.00066616 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2885045G>A , CM000686.2:g.2885045G>A GRCh38
NC_000024.9:g.2753086G>A , CM000686.1:g.2753086G>A GRCh37
NC_000024.8:g.2813086G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000652562.1:n.350-1638C>T (HSFY3P)
ENST00000515575.1:n.42+30274G>A (RPS4Y1)
Search 100 bp 5'
Search 100 bp 3'