Canonical Allele Identifier: CA337440702
Gene: RPS4Y1 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.2871427C>T
GRCh37 chrY:g.2739468C>T
gnomAD v3:
Y:2871427 C / T
gnomAD v4:
chrY-2871427-C-T
Joint Max Group AF 0.60237633 (AFR)
Genomes Max Group AF 0.60237633 (AFR)
dbSNP:
9786209
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.2871427C>T , CM000686.2:g.2871427C>T GRCh38
NC_000024.9:g.2739468C>T , CM000686.1:g.2739468C>T GRCh37
NC_000024.8:g.2799468C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000515575.1:n.42+16656C>T
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