Canonical Allele Identifier: CA337453152
Gene: RPS4Y1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.2914774G>C
GRCh37 chrY:g.2782815G>C
gnomAD v3:
Y:2914774 G / C
gnomAD v4:
chrY-2914774-G-C
Joint Max Group AF 0.00022781 (AFR)
Genomes Max Group AF 0.00022781 (AFR)
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2914774G>C , CM000686.2:g.2914774G>C GRCh38
NC_000024.9:g.2782815G>C , CM000686.1:g.2782815G>C GRCh37
NC_000024.8:g.2842815G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000515575.1:n.43-14090G>C
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