Canonical Allele Identifier: CA2000559434
Gene: SDHD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112086806A= , CM000673.2:g.112086806A= GRCh38
NC_000011.9:g.111957530A= , CM000673.1:g.111957530A= GRCh37
NC_000011.8:g.111462740A= NCBI36
NG_012337.2:g.4960A=
NG_033145.1:g.4993T=
NG_012337.3:g.4960A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375549.7:c.-102A= ENSP00000364699.3:n.-102A=