Canonical Allele Identifier: CA337440493
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs776554858
gnomAD v3: Y-2866690-A-G
gnomAD v4: Y-2866690-A-G
MyVariant Identifiers: chrY:g.2734731A>G (hg19) chrY:g.2866690A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2866690A>G , CM000686.2:g.2866690A>G GRCh38
NC_000024.9:g.2734731A>G , CM000686.1:g.2734731A>G GRCh37
NC_000024.8:g.2794731A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.691-103A>G MANE Select ENSP00000250784.7:n.691-103A>G
ENST00000250784.12:c.691-103A>G ENSP00000250784.7:n.691-103A>G
ENST00000430575.1:c.718-103A>G ENSP00000415317.1:n.718-103A>G
ENST00000477725.1:n.835-103A>G
ENST00000515575.1:n.42+11919A>G
NM_001008.3:c.691-103A>G NP_000999.1:n.691-103A>G
NM_001008.4:c.691-103A>G MANE Select NP_000999.1:n.691-103A>G
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