Canonical Allele Identifier: CA2000561859

Gene: SDHD

Linked Data

• ClinVar Variation Id: 1026388
• ClinVar RCV Id: RCV002242293
• dbSNP Id: rs753703004

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112088861T>G , CM000673.2:g.112088861T>G	GRCh38
NC_000011.9:g.111959585T>G , CM000673.1:g.111959585T>G	GRCh37
NC_000011.8:g.111464795T>G	NCBI36
NG_012337.2:g.7015T>G
NG_033145.1:g.2938A>C
NG_012337.3:g.7015T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000530923.6:c.170-6T>G	ENSP00000432946.2:n.170-6T>G
ENST00000534010.2:c.170-6T>G	ENSP00000433202.2:n.170-6T>G
ENST00000375549.8:c.170-6T>G MANE Select	ENSP00000364699.3:n.170-6T>G
ENST00000528021.6:c.170-6T>G	ENSP00000432465.1:n.170-6T>G
ENST00000640554.1:c.*242-6T>G	ENSP00000491141.1:n.*242-6T>G
ENST00000375549.7:c.170-6T>G	ENSP00000364699.3:n.170-6T>G
ENST00000525291.5:c.53-6T>G	ENSP00000436669.1:n.53-6T>G
ENST00000525987.5:n.175-6T>G
ENST00000526592.5:c.170-6T>G	ENSP00000432005.1:n.170-6T>G
ENST00000528021.5:c.170-6T>G	ENSP00000432465.1:n.170-6T>G
ENST00000528048.5:c.169+888T>G	ENSP00000436217.1:n.169+888T>G
ENST00000528182.5:c.170-6T>G	ENSP00000435475.1:n.170-6T>G
ENST00000530923.5:c.160-6T>G
ENST00000531744.5:c.170-6T>G	ENSP00000456957.1:n.170-6T>G
ENST00000532699.1:c.170-6T>G	ENSP00000456434.1:n.170-6T>G
ENST00000614349.4:c.170-6T>G	ENSP00000480666.1:n.170-6T>G
NM_001276503.1:c.169+888T>G	NP_001263432.1:n.169+888T>G
NM_001276504.1:c.53-6T>G	NP_001263433.1:n.53-6T>G
NM_001276506.1:c.170-6T>G	NP_001263435.1:n.170-6T>G
NM_003002.3:c.170-6T>G	NP_002993.1:n.170-6T>G
NR_077060.1:n.254-6T>G
NM_003002.4:c.170-6T>G MANE Select	NP_002993.1:n.170-6T>G
NM_001276503.2:c.169+888T>G	NP_001263432.1:n.169+888T>G
NM_001276504.2:c.53-6T>G	NP_001263433.1:n.53-6T>G
NM_001276506.2:c.170-6T>G	NP_001263435.1:n.170-6T>G
NR_077060.2:n.205-6T>G