Canonical Allele Identifier: CA414858152
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs1482596943
gnomAD v2: Y-22921755-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759869C>A , CM000686.2:g.20759869C>A GRCh38
NC_000024.9:g.22921755C>A , CM000686.1:g.22921755C>A GRCh37
NC_000024.8:g.21331143C>A NCBI36
NG_032924.1:g.8802C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.83C>A MANE Select ENSP00000486252.1:p.Ala28Glu
ENST00000629237.1:c.83C>A ENSP00000486252.1:p.Ala28Glu
NM_001039567.2:c.83C>A NP_001034656.1:p.Ala28Glu
XM_011531423.1:c.32C>A XP_011529725.1:p.Ala11Glu
NM_001039567.3:c.83C>A MANE Select NP_001034656.1:p.Ala28Glu