Canonical Allele Identifier: CA337439842
Gene: RPS4Y1 HGNC NCBI

Linked Data

dbSNP Id: rs999744659
gnomAD v3: Y-2843337-T-G
gnomAD v4: Y-2843337-T-G
MyVariant Identifiers: chrY:g.2711378T>G (hg19) chrY:g.2843337T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2843337T>G , CM000686.2:g.2843337T>G GRCh38
NC_000024.9:g.2711378T>G , CM000686.1:g.2711378T>G GRCh37
NC_000024.8:g.2771378T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000679518.1:n.327-740T>G
ENST00000681787.1:n.383-740T>G
ENST00000681940.1:n.107-2309T>G
ENST00000250784.13:c.82-740T>G MANE Select ENSP00000250784.7:n.82-740T>G
ENST00000250784.12:c.82-740T>G ENSP00000250784.7:n.82-740T>G
ENST00000430575.1:c.109-740T>G ENSP00000415317.1:n.109-740T>G
NM_001008.3:c.82-740T>G NP_000999.1:n.82-740T>G
NM_001008.4:c.82-740T>G MANE Select NP_000999.1:n.82-740T>G
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