Canonical Allele Identifier: CA18666435

Gene: SDHB

Linked Data

• dbSNP Id: rs764346051
• MyVariant Identifiers: chr1:g.17354887C>G (hg19) ; chr1:g.17028392C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028392C>G , CM000663.2:g.17028392C>G	GRCh38
NC_000001.10:g.17354887C>G , CM000663.1:g.17354887C>G	GRCh37
NC_000001.9:g.17227474C>G	NCBI36
NG_012340.1:g.30779G>C , LRG_316:g.30779G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.252+208G>C	ENSP00000481376.2:n.252+208G>C
ENST00000491274.6:c.381+208G>C	ENSP00000480482.2:n.381+208G>C
ENST00000375499.8:c.423+208G>C MANE Select	ENSP00000364649.3:n.423+208G>C
ENST00000375499.7:c.423+208G>C	ENSP00000364649.3:n.423+208G>C
ENST00000463045.2:c.252+208G>C	ENSP00000481376.1:n.252+208G>C
ENST00000475506.1:n.340+208G>C
ENST00000485515.5:n.357+262G>C
ENST00000491274.5:c.381+208G>C	ENSP00000480482.1:n.381+208G>C
NM_003000.2:c.423+208G>C , LRG_316t1:c.423+208G>C	NP_002991.2:n.423+208G>C
NM_003000.3:c.423+208G>C MANE Select	NP_002991.2:n.423+208G>C