Canonical Allele Identifier: CA601745101

Gene: SDHD

Linked Data

• dbSNP Id: rs1471464700
• gnomAD v2: 11-111959835-A-G
• gnomAD v3: 11-112089111-A-G
• gnomAD v4: 11-112089111-A-G
• MyVariant Identifiers: chr11:g.111959835A>G (hg19) ; chr11:g.112089111A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112089111A>G , CM000673.2:g.112089111A>G	GRCh38
NC_000011.9:g.111959835A>G , CM000673.1:g.111959835A>G	GRCh37
NC_000011.8:g.111465045A>G	NCBI36
NG_012337.2:g.7265A>G
NG_033145.1:g.2688T>C
NG_012337.3:g.7265A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.314+100A>G	ENSP00000432946.2:n.314+100A>G
ENST00000534010.2:c.314+100A>G	ENSP00000433202.2:n.314+100A>G
ENST00000375549.8:c.314+100A>G MANE Select	ENSP00000364699.3:n.314+100A>G
ENST00000528021.6:c.314+100A>G	ENSP00000432465.1:n.314+100A>G
ENST00000375549.7:c.314+100A>G	ENSP00000364699.3:n.314+100A>G
ENST00000525291.5:c.197+100A>G	ENSP00000436669.1:n.197+100A>G
ENST00000525987.5:n.319+100A>G
ENST00000526592.5:c.314+100A>G	ENSP00000432005.1:n.314+100A>G
ENST00000528021.5:c.314+100A>G	ENSP00000432465.1:n.314+100A>G
ENST00000528048.5:c.169+1138A>G	ENSP00000436217.1:n.169+1138A>G
ENST00000528182.5:c.307+107A>G	ENSP00000435475.1:n.307+107A>G
ENST00000530923.5:c.304+100A>G
ENST00000531744.5:c.314+100A>G	ENSP00000456957.1:n.314+100A>G
ENST00000532699.1:c.314+100A>G	ENSP00000456434.1:n.314+100A>G
ENST00000534010.1:c.145+100A>G
ENST00000614349.4:c.314+100A>G	ENSP00000480666.1:n.314+100A>G
NM_001276503.1:c.169+1138A>G	NP_001263432.1:n.169+1138A>G
NM_001276504.1:c.197+100A>G	NP_001263433.1:n.197+100A>G
NM_001276506.1:c.314+100A>G	NP_001263435.1:n.314+100A>G
NM_003002.3:c.314+100A>G	NP_002993.1:n.314+100A>G
NR_077060.1:n.398+100A>G
NM_003002.4:c.314+100A>G MANE Select	NP_002993.1:n.314+100A>G
NM_001276503.2:c.169+1138A>G	NP_001263432.1:n.169+1138A>G
NM_001276504.2:c.197+100A>G	NP_001263433.1:n.197+100A>G
NM_001276506.2:c.314+100A>G	NP_001263435.1:n.314+100A>G
NR_077060.2:n.349+100A>G