Canonical Allele Identifier: CA414857745
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs1198230096
gnomAD v2: Y-22918668-G-A
COSMIC: COSM5450675
MyVariant Identifiers: chrY:g.22918668G>A (hg19) chrY:g.20756782G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20756782G>A , CM000686.2:g.20756782G>A GRCh38
NC_000024.9:g.22918668G>A , CM000686.1:g.22918668G>A GRCh37
NC_000024.8:g.21328056G>A NCBI36
NG_032924.1:g.5715G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.8G>A MANE Select ENSP00000486252.1:p.Arg3Gln
ENST00000629237.1:c.8G>A ENSP00000486252.1:p.Arg3Gln
NM_001039567.2:c.8G>A NP_001034656.1:p.Arg3Gln
NM_001039567.3:c.8G>A MANE Select NP_001034656.1:p.Arg3Gln
Search 100 bp 5'
Search 100 bp 3'