Canonical Allele Identifier: CA416086149

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027824-A-C
• MyVariant Identifiers: chr1:g.17354319A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027824A>C , CM000663.2:g.17027824A>C	GRCh38
NC_000001.10:g.17354319A>C , CM000663.1:g.17354319A>C	GRCh37
NC_000001.9:g.17226906A>C	NCBI36
NG_012340.1:g.31347T>G , LRG_316:g.31347T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.294T>G	ENSP00000481376.2:p.Pro98=
ENST00000491274.6:c.423T>G	ENSP00000480482.2:p.Pro141=
ENST00000375499.8:c.465T>G MANE Select	ENSP00000364649.3:p.Pro155=
ENST00000375499.7:c.465T>G	ENSP00000364649.3:p.Pro155=
ENST00000463045.2:c.294T>G	ENSP00000481376.1:p.Pro98=
ENST00000475506.1:n.382T>G
ENST00000485515.5:n.399T>G
ENST00000491274.5:c.423T>G	ENSP00000480482.1:p.Pro141=
NM_003000.2:c.465T>G , LRG_316t1:c.465T>G	NP_002991.2:p.Pro155=
NM_003000.3:c.465T>G MANE Select	NP_002991.2:p.Pro155=