Canonical Allele Identifier: CA228550152

Gene: SDHD

Linked Data

• dbSNP Id: rs1022043662 ; rs2133523806
• gnomAD v2: 11-111957547-C-A
• gnomAD v3: 11-112086823-C-A
• gnomAD v4: 11-112086823-C-A
• MyVariant Identifiers: chr11:g.111957547C>A (hg19) ; chr11:g.112086823C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086823C>A , CM000673.2:g.112086823C>A	GRCh38
NC_000011.9:g.111957547C>A , CM000673.1:g.111957547C>A	GRCh37
NC_000011.8:g.111462757C>A	NCBI36
NG_012337.2:g.4977C>A
NG_033145.1:g.4976G>T
NG_012337.3:g.4977C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375549.7:c.-85C>A	ENSP00000364699.3:n.-85C>A