Canonical Allele Identifier: CA414947338
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734859C>A (hg19) chrY:g.2866818C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866818C>A , CM000686.2:g.2866818C>A GRCh38
NC_000024.9:g.2734859C>A , CM000686.1:g.2734859C>A GRCh37
NC_000024.8:g.2794859C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.716C>A MANE Select ENSP00000250784.7:p.Pro239His
ENST00000250784.12:c.716C>A ENSP00000250784.7:p.Pro239His
ENST00000430575.1:c.743C>A ENSP00000415317.1:p.Pro248His
ENST00000477725.1:n.860C>A
ENST00000515575.1:n.42+12047C>A
NM_001008.3:c.716C>A NP_000999.1:p.Pro239His
NM_001008.4:c.716C>A MANE Select NP_000999.1:p.Pro239His
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