Canonical Allele Identifier: CA414858439
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs1569396231
MyVariant Identifiers: chrY:g.22921827T>C (hg19) chrY:g.20759941T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759941T>C , CM000686.2:g.20759941T>C GRCh38
NC_000024.9:g.22921827T>C , CM000686.1:g.22921827T>C GRCh37
NC_000024.8:g.21331215T>C NCBI36
NG_032924.1:g.8874T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.155T>C MANE Select ENSP00000486252.1:p.Leu52Pro
ENST00000629237.1:c.155T>C ENSP00000486252.1:p.Leu52Pro
NM_001039567.2:c.155T>C NP_001034656.1:p.Leu52Pro
XM_011531423.1:c.104T>C XP_011529725.1:p.Leu35Pro
NM_001039567.3:c.155T>C MANE Select NP_001034656.1:p.Leu52Pro
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