Canonical Allele Identifier: CA519439348
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734906A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866865A>C , CM000686.2:g.2866865A>C GRCh38
NC_000024.9:g.2734906A>C , CM000686.1:g.2734906A>C GRCh37
NC_000024.8:g.2794906A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.763A>C MANE Select ENSP00000250784.7:p.Arg255=
ENST00000250784.12:c.763A>C ENSP00000250784.7:p.Arg255=
ENST00000477725.1:n.907A>C
ENST00000515575.1:n.42+12094A>C
NM_001008.3:c.763A>C NP_000999.1:p.Arg255=
NM_001008.4:c.763A>C MANE Select NP_000999.1:p.Arg255=