Canonical Allele Identifier: CA519439357
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734917C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866876C>A , CM000686.2:g.2866876C>A GRCh38
NC_000024.9:g.2734917C>A , CM000686.1:g.2734917C>A GRCh37
NC_000024.8:g.2794917C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.774C>A MANE Select ENSP00000250784.7:p.Thr258=
ENST00000250784.12:c.774C>A ENSP00000250784.7:p.Thr258=
ENST00000477725.1:n.918C>A
ENST00000515575.1:n.42+12105C>A
NM_001008.3:c.774C>A NP_000999.1:p.Thr258=
NM_001008.4:c.774C>A MANE Select NP_000999.1:p.Thr258=