Canonical Allele Identifier: CA414858210
Gene: RPS4Y2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.22921770C>A (hg19) chrY:g.20759884C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759884C>A , CM000686.2:g.20759884C>A GRCh38
NC_000024.9:g.22921770C>A , CM000686.1:g.22921770C>A GRCh37
NC_000024.8:g.21331158C>A NCBI36
NG_032924.1:g.8817C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.98C>A MANE Select ENSP00000486252.1:p.Thr33Lys
ENST00000629237.1:c.98C>A ENSP00000486252.1:p.Thr33Lys
NM_001039567.2:c.98C>A NP_001034656.1:p.Thr33Lys
XM_011531423.1:c.47C>A XP_011529725.1:p.Thr16Lys
NM_001039567.3:c.98C>A MANE Select NP_001034656.1:p.Thr33Lys
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