Canonical Allele Identifier: CA519439296
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734836C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866795C>T , CM000686.2:g.2866795C>T GRCh38
NC_000024.9:g.2734836C>T , CM000686.1:g.2734836C>T GRCh37
NC_000024.8:g.2794836C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.693C>T MANE Select ENSP00000250784.7:p.Gly231=
ENST00000250784.12:c.693C>T ENSP00000250784.7:p.Gly231=
ENST00000430575.1:c.720C>T ENSP00000415317.1:p.Gly240=
ENST00000477725.1:n.837C>T
ENST00000515575.1:n.42+12024C>T
NM_001008.3:c.693C>T NP_000999.1:p.Gly231=
NM_001008.4:c.693C>T MANE Select NP_000999.1:p.Gly231=