Canonical Allele Identifier: CA476789157

Gene: SDHD

Linked Data

• ClinVar Variation Id: 755556
• ClinVar RCV Id: RCV002235696 ; RCV002354795
• dbSNP Id: rs1566690237
• gnomAD v4: 11-112086946-C-T
• MyVariant Identifiers: chr11:g.111957670C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086946C>T , CM000673.2:g.112086946C>T	GRCh38
NC_000011.9:g.111957670C>T , CM000673.1:g.111957670C>T	GRCh37
NC_000011.8:g.111462880C>T	NCBI36
NG_012337.2:g.5100C>T
NG_033145.1:g.4853G>A
NG_012337.3:g.5100C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.39C>T	ENSP00000432946.2:p.Ala13=
ENST00000534010.2:c.39C>T	ENSP00000433202.2:p.Ala13=
ENST00000375549.8:c.39C>T MANE Select	ENSP00000364699.3:p.Ala13=
ENST00000528021.6:c.39C>T	ENSP00000432465.1:p.Ala13=
ENST00000640554.1:c.39C>T	ENSP00000491141.1:p.Ala13=
ENST00000375549.7:c.39C>T	ENSP00000364699.3:p.Ala13=
ENST00000525291.5:c.39C>T	ENSP00000436669.1:p.Ala13=
ENST00000525987.5:n.44C>T
ENST00000526592.5:c.39C>T	ENSP00000432005.1:p.Ala13=
ENST00000528021.5:c.39C>T	ENSP00000432465.1:p.Ala13=
ENST00000528048.5:c.39C>T	ENSP00000436217.1:p.Ala13=
ENST00000528182.5:c.39C>T	ENSP00000435475.1:p.Ala13=
ENST00000530923.5:c.29C>T
ENST00000531744.5:c.39C>T	ENSP00000456957.1:p.Ala13=
ENST00000532699.1:c.39C>T	ENSP00000456434.1:p.Ala13=
ENST00000614349.4:c.39C>T	ENSP00000480666.1:p.Ala13=
NM_001276503.1:c.39C>T	NP_001263432.1:p.Ala13=
NM_001276504.1:c.39C>T	NP_001263433.1:p.Ala13=
NM_001276506.1:c.39C>T	NP_001263435.1:p.Ala13=
NM_003002.3:c.39C>T	NP_002993.1:p.Ala13=
NR_077060.1:n.123C>T
NM_003002.4:c.39C>T MANE Select	NP_002993.1:p.Ala13=
NM_001276503.2:c.39C>T	NP_001263432.1:p.Ala13=
NM_001276504.2:c.39C>T	NP_001263433.1:p.Ala13=
NM_001276506.2:c.39C>T	NP_001263435.1:p.Ala13=
NR_077060.2:n.74C>T