Canonical Allele Identifier: CA520176162
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921756A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759870A>G , CM000686.2:g.20759870A>G GRCh38
NC_000024.9:g.22921756A>G , CM000686.1:g.22921756A>G GRCh37
NC_000024.8:g.21331144A>G NCBI36
NG_032924.1:g.8803A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.84A>G MANE Select ENSP00000486252.1:p.Ala28=
ENST00000629237.1:c.84A>G ENSP00000486252.1:p.Ala28=
NM_001039567.2:c.84A>G NP_001034656.1:p.Ala28=
XM_011531423.1:c.33A>G XP_011529725.1:p.Ala11=
NM_001039567.3:c.84A>G MANE Select NP_001034656.1:p.Ala28=