Canonical Allele Identifier: CA520176227
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921771A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759885A>T , CM000686.2:g.20759885A>T GRCh38
NC_000024.9:g.22921771A>T , CM000686.1:g.22921771A>T GRCh37
NC_000024.8:g.21331159A>T NCBI36
NG_032924.1:g.8818A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.99A>T MANE Select ENSP00000486252.1:p.Thr33=
ENST00000629237.1:c.99A>T ENSP00000486252.1:p.Thr33=
NM_001039567.2:c.99A>T NP_001034656.1:p.Thr33=
XM_011531423.1:c.48A>T XP_011529725.1:p.Thr16=
NM_001039567.3:c.99A>T MANE Select NP_001034656.1:p.Thr33=