Canonical Allele Identifier: CA1140178327
Gene: MTND2P28 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.630216G= , CM000663.2:g.630216G= GRCh38
NC_000001.10:g.565596G= , CM000663.1:g.565596G= GRCh37
NC_000001.9:g.555459G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419394.2:n.481-43261C=
ENST00000440196.3:n.87-1210C=
ENST00000440200.5:n.170-22160C=
ENST00000452176.2:n.20+915C=
ENST00000634337.2:n.161-22160C=
ENST00000635509.2:n.313-28639C=
ENST00000641296.1:n.74+915C=
ENST00000648019.1:n.636-22160C=
ENST00000457540.1:n.577G=