Canonical Allele Identifier: CA601744382

Gene: SDHD

Linked Data

• dbSNP Id: rs764936238
• gnomAD v2: 11-111957611-C-T
• gnomAD v3: 11-112086887-C-T
• gnomAD v4: 11-112086887-C-T
• MyVariant Identifiers: chr11:g.111957611C>T (hg19) ; chr11:g.112086887C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112086887C>T , CM000673.2:g.112086887C>T	GRCh38
NC_000011.9:g.111957611C>T , CM000673.1:g.111957611C>T	GRCh37
NC_000011.8:g.111462821C>T	NCBI36
NG_012337.2:g.5041C>T
NG_033145.1:g.4912G>A
NG_012337.3:g.5041C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000530923.6:c.-21C>T	ENSP00000432946.2:n.-21C>T
ENST00000534010.2:c.-21C>T	ENSP00000433202.2:n.-21C>T
ENST00000375549.8:c.-21C>T MANE Select	ENSP00000364699.3:n.-21C>T
ENST00000528021.6:c.-21C>T	ENSP00000432465.1:n.-21C>T
ENST00000640554.1:c.-21C>T	ENSP00000491141.1:n.-21C>T
ENST00000375549.7:c.-21C>T	ENSP00000364699.3:n.-21C>T
ENST00000528021.5:c.-21C>T	ENSP00000432465.1:n.-21C>T
ENST00000528048.5:c.-21C>T	ENSP00000436217.1:n.-21C>T
ENST00000528182.5:c.-21C>T	ENSP00000435475.1:n.-21C>T
ENST00000614349.4:c.-21C>T	ENSP00000480666.1:n.-21C>T
NM_001276503.1:c.-21C>T	NP_001263432.1:n.-21C>T
NM_001276504.1:c.-21C>T	NP_001263433.1:n.-21C>T
NM_001276506.1:c.-21C>T	NP_001263435.1:n.-21C>T
NM_003002.3:c.-21C>T	NP_002993.1:n.-21C>T
NR_077060.1:n.64C>T
NM_003002.4:c.-21C>T MANE Select	NP_002993.1:n.-21C>T
NM_001276503.2:c.-21C>T	NP_001263432.1:n.-21C>T
NM_001276504.2:c.-21C>T	NP_001263433.1:n.-21C>T
NM_001276506.2:c.-21C>T	NP_001263435.1:n.-21C>T
NR_077060.2:n.15C>T