Canonical Allele Identifier: CA10575188
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs747890808
ExAC: Y:22921786 G / A
gnomAD v2: Y-22921786-G-A
MyVariant Identifiers: chrY:g.22921786G>A (hg19) chrY:g.20759900G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759900G>A , CM000686.2:g.20759900G>A GRCh38
NC_000024.9:g.22921786G>A , CM000686.1:g.22921786G>A GRCh37
NC_000024.8:g.21331174G>A NCBI36
NG_032924.1:g.8833G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.114G>A MANE Select ENSP00000486252.1:p.Leu38=
ENST00000629237.1:c.114G>A ENSP00000486252.1:p.Leu38=
NM_001039567.2:c.114G>A NP_001034656.1:p.Leu38=
XM_011531423.1:c.63G>A XP_011529725.1:p.Leu21=
NM_001039567.3:c.114G>A MANE Select NP_001034656.1:p.Leu38=
Search 100 bp 5'
Search 100 bp 3'