Canonical Allele Identifier: CA337440200
Gene: RPS4Y1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.2856465T>G
GRCh37 chrY:g.2724506T>G
gnomAD v3:
Y:2856465 T / G
gnomAD v4:
chrY-2856465-T-G
Joint Max Group AF 0.00805446 (NFE)
Genomes Max Group AF 0.00805446 (NFE)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2856465T>G , CM000686.2:g.2856465T>G GRCh38
NC_000024.9:g.2724506T>G , CM000686.1:g.2724506T>G GRCh37
NC_000024.8:g.2784506T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000250784.13:c.532+1694T>G MANE Select ENSP00000250784.7:n.532+1694T>G
ENST00000250784.12:c.532+1694T>G ENSP00000250784.7:n.532+1694T>G
ENST00000430575.1:c.559+1694T>G ENSP00000415317.1:n.559+1694T>G
ENST00000477725.1:n.676+1694T>G
ENST00000515575.1:n.42+1694T>G
NM_001008.3:c.532+1694T>G NP_000999.1:n.532+1694T>G
NM_001008.4:c.532+1694T>G MANE Select NP_000999.1:n.532+1694T>G
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