Canonical Allele Identifier: CA337618387
Gene: MTND2P3 HGNC NCBI

Linked Data

dbSNP Id: rs34761704
gnomAD v3: Y-8372684-C-T
gnomAD v4: Y-8372684-C-T
MyVariant Identifiers: chrY:g.8240725C>T (hg19) chrY:g.8372684C>T (hg38)
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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
Search 100 bp 5'
Search 100 bp 3'