Canonical Allele Identifier: CA18662035

Gene: SDHB

Linked Data

• dbSNP Id: rs910713015
• gnomAD v2: 1-17349023-C-T
• gnomAD v3: 1-17022528-C-T
• gnomAD v4: 1-17022528-C-T
• MyVariant Identifiers: chr1:g.17349023C>T (hg19) ; chr1:g.17022528C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022528C>T , CM000663.2:g.17022528C>T	GRCh38
NC_000001.10:g.17349023C>T , CM000663.1:g.17349023C>T	GRCh37
NC_000001.9:g.17221610C>T	NCBI36
NG_012340.1:g.36643G>A , LRG_316:g.36643G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+80G>A	ENSP00000481376.2:n.594+80G>A
ENST00000491274.6:c.723+80G>A	ENSP00000480482.2:n.723+80G>A
ENST00000375499.8:c.765+80G>A MANE Select	ENSP00000364649.3:n.765+80G>A
ENST00000375499.7:c.765+80G>A	ENSP00000364649.3:n.765+80G>A
ENST00000475049.5:n.190+80G>A
ENST00000485092.5:n.429+80G>A
NM_003000.2:c.765+80G>A , LRG_316t1:c.765+80G>A	NP_002991.2:n.765+80G>A
NM_003000.3:c.765+80G>A MANE Select	NP_002991.2:n.765+80G>A