Canonical Allele Identifier: CA089623

Gene: SDHB

Linked Data

• dbSNP Id: rs751173676
• ExAC: 1:17354403 T / C
• gnomAD v2: 1-17354403-T-C
• gnomAD v4: 1-17027908-T-C
• MyVariant Identifiers: chr1:g.17354403T>C (hg19) ; chr1:g.17027908T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027908T>C , CM000663.2:g.17027908T>C	GRCh38
NC_000001.10:g.17354403T>C , CM000663.1:g.17354403T>C	GRCh37
NC_000001.9:g.17226990T>C	NCBI36
NG_012340.1:g.31263A>G , LRG_316:g.31263A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.253-43A>G	ENSP00000481376.2:n.253-43A>G
ENST00000491274.6:c.382-43A>G	ENSP00000480482.2:n.382-43A>G
ENST00000375499.8:c.424-43A>G MANE Select	ENSP00000364649.3:n.424-43A>G
ENST00000375499.7:c.424-43A>G	ENSP00000364649.3:n.424-43A>G
ENST00000463045.2:c.253-43A>G	ENSP00000481376.1:n.253-43A>G
ENST00000475506.1:n.341-43A>G
ENST00000485515.5:n.358-43A>G
ENST00000491274.5:c.382-43A>G	ENSP00000480482.1:n.382-43A>G
NM_003000.2:c.424-43A>G , LRG_316t1:c.424-43A>G	NP_002991.2:n.424-43A>G
NM_003000.3:c.424-43A>G MANE Select	NP_002991.2:n.424-43A>G