Canonical Allele Identifier: CA2471054988
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs2089439362

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20769237A>G , CM000686.2:g.20769237A>G GRCh38
NC_000024.9:g.22931123A>G , CM000686.1:g.22931123A>G GRCh37
NC_000024.8:g.21340511A>G NCBI36
NG_032924.1:g.18170A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.532+261A>G MANE Select ENSP00000486252.1:n.532+261A>G
ENST00000629237.1:c.532+261A>G ENSP00000486252.1:n.532+261A>G
NM_001039567.2:c.532+261A>G NP_001034656.1:n.532+261A>G
XM_011531423.1:c.481+261A>G XP_011529725.1:n.481+261A>G
NM_001039567.3:c.532+261A>G MANE Select NP_001034656.1:n.532+261A>G