Canonical Allele Identifier: CA337440498
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs868448356
MyVariant Identifiers: chrY:g.2734919A>G (hg19) chrY:g.2866878A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866878A>G , CM000686.2:g.2866878A>G GRCh38
NC_000024.9:g.2734919A>G , CM000686.1:g.2734919A>G GRCh37
NC_000024.8:g.2794919A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.776A>G MANE Select ENSP00000250784.7:p.Lys259Arg
ENST00000250784.12:c.776A>G ENSP00000250784.7:p.Lys259Arg
ENST00000477725.1:n.920A>G
ENST00000515575.1:n.42+12107A>G
NM_001008.3:c.776A>G NP_000999.1:p.Lys259Arg
NM_001008.4:c.776A>G MANE Select NP_000999.1:p.Lys259Arg
Search 100 bp 5'
Search 100 bp 3'