Canonical Allele Identifier: CA520176537
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921846A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759960A>T , CM000686.2:g.20759960A>T GRCh38
NC_000024.9:g.22921846A>T , CM000686.1:g.22921846A>T GRCh37
NC_000024.8:g.21331234A>T NCBI36
NG_032924.1:g.8893A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.174A>T MANE Select ENSP00000486252.1:p.Gly58=
ENST00000629237.1:c.174A>T ENSP00000486252.1:p.Gly58=
NM_001039567.2:c.174A>T NP_001034656.1:p.Gly58=
XM_011531423.1:c.123A>T XP_011529725.1:p.Gly41=
NM_001039567.3:c.174A>T MANE Select NP_001034656.1:p.Gly58=