Canonical Allele Identifier: CA520176236
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921774T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759888T>A , CM000686.2:g.20759888T>A GRCh38
NC_000024.9:g.22921774T>A , CM000686.1:g.22921774T>A GRCh37
NC_000024.8:g.21331162T>A NCBI36
NG_032924.1:g.8821T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.102T>A MANE Select ENSP00000486252.1:p.Gly34=
ENST00000629237.1:c.102T>A ENSP00000486252.1:p.Gly34=
NM_001039567.2:c.102T>A NP_001034656.1:p.Gly34=
XM_011531423.1:c.51T>A XP_011529725.1:p.Gly17=
NM_001039567.3:c.102T>A MANE Select NP_001034656.1:p.Gly34=