Canonical Allele Identifier: CA880352198
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs1344254665
MyVariant Identifiers: chrY:g.2713534T>C (hg19) chrY:g.2845493T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2845493T>C , CM000686.2:g.2845493T>C GRCh38
NC_000024.9:g.2713534T>C , CM000686.1:g.2713534T>C GRCh37
NC_000024.8:g.2773534T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000679518.1:n.508-153T>C
ENST00000681787.1:n.564-153T>C
ENST00000681940.1:n.107-153T>C
ENST00000250784.13:c.263-153T>C MANE Select ENSP00000250784.7:n.263-153T>C
ENST00000250784.12:c.263-153T>C ENSP00000250784.7:n.263-153T>C
ENST00000430575.1:c.290-153T>C ENSP00000415317.1:n.290-153T>C
NM_001008.3:c.263-153T>C NP_000999.1:n.263-153T>C
NM_001008.4:c.263-153T>C MANE Select NP_000999.1:n.263-153T>C
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