Canonical Allele Identifier: CA519439298
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734836C>G (hg19)
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Genomic Alleles

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

Transcript Alleles

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