Canonical Allele Identifier: CA519439335
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734884T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866843T>G , CM000686.2:g.2866843T>G GRCh38
NC_000024.9:g.2734884T>G , CM000686.1:g.2734884T>G GRCh37
NC_000024.8:g.2794884T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.741T>G MANE Select ENSP00000250784.7:p.Thr247=
ENST00000250784.12:c.741T>G ENSP00000250784.7:p.Thr247=
ENST00000430575.1:c.768T>G ENSP00000415317.1:p.Thr256=
ENST00000477725.1:n.885T>G
ENST00000515575.1:n.42+12072T>G
NM_001008.3:c.741T>G NP_000999.1:p.Thr247=
NM_001008.4:c.741T>G MANE Select NP_000999.1:p.Thr247=