Canonical Allele Identifier: CA520176459
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921825A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759939A>G , CM000686.2:g.20759939A>G GRCh38
NC_000024.9:g.22921825A>G , CM000686.1:g.22921825A>G GRCh37
NC_000024.8:g.21331213A>G NCBI36
NG_032924.1:g.8872A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.153A>G MANE Select ENSP00000486252.1:p.Arg51=
ENST00000629237.1:c.153A>G ENSP00000486252.1:p.Arg51=
NM_001039567.2:c.153A>G NP_001034656.1:p.Arg51=
XM_011531423.1:c.102A>G XP_011529725.1:p.Arg34=
NM_001039567.3:c.153A>G MANE Select NP_001034656.1:p.Arg51=