Canonical Allele Identifier: CA089621

Gene: SDHB

Linked Data

• dbSNP Id: rs757911908
• ExAC: 1:17354400 G / C
• gnomAD v2: 1-17354400-G-C
• gnomAD v4: 1-17027905-G-C
• MyVariant Identifiers: chr1:g.17354400G>C (hg19) ; chr1:g.17027905G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027905G>C , CM000663.2:g.17027905G>C	GRCh38
NC_000001.10:g.17354400G>C , CM000663.1:g.17354400G>C	GRCh37
NC_000001.9:g.17226987G>C	NCBI36
NG_012340.1:g.31266C>G , LRG_316:g.31266C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.253-40C>G	ENSP00000481376.2:n.253-40C>G
ENST00000491274.6:c.382-40C>G	ENSP00000480482.2:n.382-40C>G
ENST00000375499.8:c.424-40C>G MANE Select	ENSP00000364649.3:n.424-40C>G
ENST00000375499.7:c.424-40C>G	ENSP00000364649.3:n.424-40C>G
ENST00000463045.2:c.253-40C>G	ENSP00000481376.1:n.253-40C>G
ENST00000475506.1:n.341-40C>G
ENST00000485515.5:n.358-40C>G
ENST00000491274.5:c.382-40C>G	ENSP00000480482.1:n.382-40C>G
NM_003000.2:c.424-40C>G , LRG_316t1:c.424-40C>G	NP_002991.2:n.424-40C>G
NM_003000.3:c.424-40C>G MANE Select	NP_002991.2:n.424-40C>G