Canonical Allele Identifier: CA337440088
Gene: RPS4Y1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.2854211G>A
GRCh37 chrY:g.2722252G>A
gnomAD v3:
Y:2854211 G / A
gnomAD v4:
chrY-2854211-G-A
Joint Max Group AF 0.00060207 (AFR)
Genomes Max Group AF 0.00046214 (AFR)
Exomes Max Group AF 0.00087229 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2854211G>A , CM000686.2:g.2854211G>A GRCh38
NC_000024.9:g.2722252G>A , CM000686.1:g.2722252G>A GRCh37
NC_000024.8:g.2782252G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000681940.1:n.205-389G>A
ENST00000250784.13:c.361-389G>A MANE Select ENSP00000250784.7:n.361-389G>A
ENST00000250784.12:c.361-389G>A ENSP00000250784.7:n.361-389G>A
ENST00000430575.1:c.388-389G>A ENSP00000415317.1:n.388-389G>A
ENST00000477725.1:n.116G>A
NM_001008.3:c.361-389G>A NP_000999.1:n.361-389G>A
NM_001008.4:c.361-389G>A MANE Select NP_000999.1:n.361-389G>A
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