Canonical Allele Identifier: CA10575184
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs780083775
ExAC: Y:22921761 G / A
gnomAD v2: Y-22921761-G-A
COSMIC: COSM4966561
MyVariant Identifiers: chrY:g.22921761G>A (hg19) chrY:g.20759875G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759875G>A , CM000686.2:g.20759875G>A GRCh38
NC_000024.9:g.22921761G>A , CM000686.1:g.22921761G>A GRCh37
NC_000024.8:g.21331149G>A NCBI36
NG_032924.1:g.8808G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.89G>A MANE Select ENSP00000486252.1:p.Arg30His
ENST00000629237.1:c.89G>A ENSP00000486252.1:p.Arg30His
NM_001039567.2:c.89G>A NP_001034656.1:p.Arg30His
XM_011531423.1:c.38G>A XP_011529725.1:p.Arg13His
NM_001039567.3:c.89G>A MANE Select NP_001034656.1:p.Arg30His
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