Canonical Allele Identifier: CA337511164
Gene: RPS4Y2 HGNC NCBI

Linked Data

dbSNP Id: rs763006446
MyVariant Identifiers: chrY:g.22922110A>G (hg19) chrY:g.20760224A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.20760224A>G , CM000686.2:g.20760224A>G GRCh38
NC_000024.9:g.22922110A>G , CM000686.1:g.22922110A>G GRCh37
NC_000024.8:g.21331498A>G NCBI36
NG_032924.1:g.9157A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000629237.2:c.262+176A>G MANE Select ENSP00000486252.1:n.262+176A>G
ENST00000629237.1:c.262+176A>G ENSP00000486252.1:n.262+176A>G
NM_001039567.2:c.262+176A>G NP_001034656.1:n.262+176A>G
XM_011531423.1:c.211+176A>G XP_011529725.1:n.211+176A>G
NM_001039567.3:c.262+176A>G MANE Select NP_001034656.1:n.262+176A>G
Search 100 bp 5'
Search 100 bp 3'