Canonical Allele Identifier: CA337618387
Gene: MTND2P3 HGNC NCBI
MyVariant.info:
GRCh38 chrY:g.8372684C>T
GRCh37 chrY:g.8240725C>T
gnomAD v3:
Y:8372684 C / T
gnomAD v4:
chrY-8372684-C-T
Joint Max Group AF 0.11920995 (MID)
Genomes Max Group AF 0.04973693 (AMR)
dbSNP:
34761704
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Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8372684C>T , CM000686.2:g.8372684C>T GRCh38
NC_000024.9:g.8240725C>T , CM000686.1:g.8240725C>T GRCh37
NC_000024.8:g.8300725C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000452458.1:n.444C>T
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