Canonical Allele Identifier: CA071292

Gene: SDHD

Linked Data

• dbSNP Id: rs200063990
• ExAC: 11:111957597 G / T
• gnomAD v2: 11-111957597-G-T
• gnomAD v3: 11-112086873-G-T
• gnomAD v4: 11-112086873-G-T
• MyVariant Identifiers: chr11:g.111957597G>T (hg19) ; chr11:g.112086873G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086873G>T , CM000673.2:g.112086873G>T	GRCh38
NC_000011.9:g.111957597G>T , CM000673.1:g.111957597G>T	GRCh37
NC_000011.8:g.111462807G>T	NCBI36
NG_012337.2:g.5027G>T
NG_033145.1:g.4926C>A
NG_012337.3:g.5027G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.-35G>T	ENSP00000432946.2:n.-35G>T
ENST00000534010.2:c.-35G>T	ENSP00000433202.2:n.-35G>T
ENST00000375549.8:c.-35G>T MANE Select	ENSP00000364699.3:n.-35G>T
ENST00000528021.6:c.-35G>T	ENSP00000432465.1:n.-35G>T
ENST00000640554.1:c.-35G>T	ENSP00000491141.1:n.-35G>T
ENST00000375549.7:c.-35G>T	ENSP00000364699.3:n.-35G>T
ENST00000528021.5:c.-35G>T	ENSP00000432465.1:n.-35G>T
ENST00000528048.5:c.-35G>T	ENSP00000436217.1:n.-35G>T
ENST00000528182.5:c.-35G>T	ENSP00000435475.1:n.-35G>T
ENST00000614349.4:c.-35G>T	ENSP00000480666.1:n.-35G>T
NM_001276503.1:c.-35G>T	NP_001263432.1:n.-35G>T
NM_001276504.1:c.-35G>T	NP_001263433.1:n.-35G>T
NM_001276506.1:c.-35G>T	NP_001263435.1:n.-35G>T
NM_003002.3:c.-35G>T	NP_002993.1:n.-35G>T
NR_077060.1:n.50G>T
NM_003002.4:c.-35G>T MANE Select	NP_002993.1:n.-35G>T
NM_001276503.2:c.-35G>T	NP_001263432.1:n.-35G>T
NM_001276504.2:c.-35G>T	NP_001263433.1:n.-35G>T
NM_001276506.2:c.-35G>T	NP_001263435.1:n.-35G>T
NR_077060.2:n.1G>T