Canonical Allele Identifier: CA671750626

Gene: SDHD

Linked Data

• dbSNP Id: rs1325181107
• gnomAD v4: 11-112095187-A-T
• MyVariant Identifiers: chr11:g.111965911A>T (hg19) ; chr11:g.112095187A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112095187A>T , CM000673.2:g.112095187A>T	GRCh38
NC_000011.9:g.111965911A>T , CM000673.1:g.111965911A>T	GRCh37
NC_000011.8:g.111471121A>T	NCBI36
NG_012337.2:g.13341A>T
NG_012337.3:g.13341A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000534010.2:c.314+6176A>T	ENSP00000433202.2:n.314+6176A>T
ENST00000375549.8:c.*217A>T MANE Select	ENSP00000364699.3:n.*217A>T
ENST00000528021.6:c.314+6176A>T	ENSP00000432465.1:n.314+6176A>T
ENST00000375549.7:c.*217A>T	ENSP00000364699.3:n.*217A>T
ENST00000525291.5:c.*217A>T	ENSP00000436669.1:n.*217A>T
ENST00000525987.5:n.319+6176A>T
ENST00000526592.5:c.*395A>T	ENSP00000432005.1:n.*395A>T
ENST00000528021.5:c.314+6176A>T	ENSP00000432465.1:n.314+6176A>T
ENST00000528048.5:c.*294A>T	ENSP00000436217.1:n.*294A>T
ENST00000528182.5:c.*294A>T	ENSP00000435475.1:n.*294A>T
ENST00000531744.5:c.314+6176A>T	ENSP00000456957.1:n.314+6176A>T
ENST00000532699.1:c.314+6176A>T	ENSP00000456434.1:n.314+6176A>T
ENST00000534010.1:c.145+6176A>T
NM_001276503.1:c.*294A>T	NP_001263432.1:n.*294A>T
NM_001276504.1:c.*217A>T	NP_001263433.1:n.*217A>T
NM_001276506.1:c.*395A>T	NP_001263435.1:n.*395A>T
NM_003002.3:c.*217A>T	NP_002993.1:n.*217A>T
NR_077060.1:n.835A>T
NM_003002.4:c.*217A>T MANE Select	NP_002993.1:n.*217A>T
NM_001276503.2:c.*294A>T	NP_001263432.1:n.*294A>T
NM_001276504.2:c.*217A>T	NP_001263433.1:n.*217A>T
NM_001276506.2:c.*395A>T	NP_001263435.1:n.*395A>T
NR_077060.2:n.786A>T