Canonical Allele Identifier: CA414947705
Gene: RPS4Y1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.2734934A>C (hg19) chrY:g.2866893A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866893A>C , CM000686.2:g.2866893A>C GRCh38
NC_000024.9:g.2734934A>C , CM000686.1:g.2734934A>C GRCh37
NC_000024.8:g.2794934A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.791A>C MANE Select ENSP00000250784.7:p.Ter264Ser
ENST00000250784.12:c.791A>C ENSP00000250784.7:p.Ter264Ser
ENST00000477725.1:n.935A>C
ENST00000515575.1:n.42+12122A>C
NM_001008.3:c.791A>C NP_000999.1:p.Ter264Ser
NM_001008.4:c.791A>C MANE Select NP_000999.1:p.Ter264Ser
Search 100 bp 5'
Search 100 bp 3'