Canonical Allele Identifier: CA2000559446
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086818C= , CM000673.2:g.112086818C= GRCh38
NC_000011.9:g.111957542C= , CM000673.1:g.111957542C= GRCh37
NC_000011.8:g.111462752C= NCBI36
NG_012337.2:g.4972C=
NG_033145.1:g.4981G=
NG_012337.3:g.4972C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375549.7:c.-90C= ENSP00000364699.3:n.-90C=