Canonical Allele Identifier: CA337532894
Gene:
dbSNP:
17250535
2124007622
2124007628
2124007637
gnomAD v4:
chrY-21311315-T-A
Joint Max Group AF 0.18174675 (SAS)
Exomes Max Group AF 0.31307834 (SAS)
MyVariant.info:
GRCh38 chrY:g.21311315T>A
GRCh37 chrY:g.23473201T>A
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.21311315T>A , CM000686.2:g.21311315T>A GRCh38
NC_000024.9:g.23473201T>A , CM000686.1:g.23473201T>A GRCh37
NC_000024.8:g.21882589T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000437359.1:n.48T>A
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