Canonical Allele Identifier: CA520176466
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921828C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759942C>G , CM000686.2:g.20759942C>G GRCh38
NC_000024.9:g.22921828C>G , CM000686.1:g.22921828C>G GRCh37
NC_000024.8:g.21331216C>G NCBI36
NG_032924.1:g.8875C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.156C>G MANE Select ENSP00000486252.1:p.Leu52=
ENST00000629237.1:c.156C>G ENSP00000486252.1:p.Leu52=
NM_001039567.2:c.156C>G NP_001034656.1:p.Leu52=
XM_011531423.1:c.105C>G XP_011529725.1:p.Leu35=
NM_001039567.3:c.156C>G MANE Select NP_001034656.1:p.Leu52=
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