Canonical Allele Identifier: CA414947573
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734915A>C (hg19) chrY:g.2866874A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866874A>C , CM000686.2:g.2866874A>C GRCh38
NC_000024.9:g.2734915A>C , CM000686.1:g.2734915A>C GRCh37
NC_000024.8:g.2794915A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.772A>C MANE Select ENSP00000250784.7:p.Thr258Pro
ENST00000250784.12:c.772A>C ENSP00000250784.7:p.Thr258Pro
ENST00000477725.1:n.916A>C
ENST00000515575.1:n.42+12103A>C
NM_001008.3:c.772A>C NP_000999.1:p.Thr258Pro
NM_001008.4:c.772A>C MANE Select NP_000999.1:p.Thr258Pro
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