Canonical Allele Identifier: CA10575176
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs764466453
gnomAD v2: Y-22921706-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20759820A>G , CM000686.2:g.20759820A>G GRCh38
NC_000024.9:g.22921706A>G , CM000686.1:g.22921706A>G GRCh37
NC_000024.8:g.21331094A>G NCBI36
NG_032924.1:g.8753A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000629237.2:c.82-48A>G MANE Select ENSP00000486252.1:n.82-48A>G
ENST00000629237.1:c.82-48A>G ENSP00000486252.1:n.82-48A>G
NM_001039567.2:c.82-48A>G NP_001034656.1:n.82-48A>G
XM_011531423.1:c.31-48A>G XP_011529725.1:n.31-48A>G
NM_001039567.3:c.82-48A>G MANE Select NP_001034656.1:n.82-48A>G