Canonical Allele Identifier: CA999081927

Gene: SDHB

Linked Data

• dbSNP Id: rs2077969852
• gnomAD v3: 1-17022860-T-A
• gnomAD v4: 1-17022860-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022860T>A , CM000663.2:g.17022860T>A	GRCh38
NC_000001.10:g.17349355T>A , CM000663.1:g.17349355T>A	GRCh37
NC_000001.9:g.17221942T>A	NCBI36
NG_012340.1:g.36311A>T , LRG_316:g.36311A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.472-130A>T	ENSP00000481376.2:n.472-130A>T
ENST00000491274.6:c.601-130A>T	ENSP00000480482.2:n.601-130A>T
ENST00000375499.8:c.643-130A>T MANE Select	ENSP00000364649.3:n.643-130A>T
ENST00000375499.7:c.643-130A>T	ENSP00000364649.3:n.643-130A>T
ENST00000475049.5:n.68-130A>T
ENST00000485092.5:n.177A>T
ENST00000485515.5:n.577-130A>T
NM_003000.2:c.643-130A>T , LRG_316t1:c.643-130A>T	NP_002991.2:n.643-130A>T
NM_003000.3:c.643-130A>T MANE Select	NP_002991.2:n.643-130A>T