Canonical Allele Identifier: CA10575189
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs771332250
ExAC: Y:22921792 A / T
gnomAD v2: Y-22921792-A-T
MyVariant Identifiers: chrY:g.22921792A>T (hg19) chrY:g.20759906A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759906A>T , CM000686.2:g.20759906A>T GRCh38
NC_000024.9:g.22921792A>T , CM000686.1:g.22921792A>T GRCh37
NC_000024.8:g.21331180A>T NCBI36
NG_032924.1:g.8839A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.120A>T MANE Select ENSP00000486252.1:p.Glu40Asp
ENST00000629237.1:c.120A>T ENSP00000486252.1:p.Glu40Asp
NM_001039567.2:c.120A>T NP_001034656.1:p.Glu40Asp
XM_011531423.1:c.69A>T XP_011529725.1:p.Glu23Asp
NM_001039567.3:c.120A>T MANE Select NP_001034656.1:p.Glu40Asp
Search 100 bp 5'
Search 100 bp 3'