Canonical Allele Identifier: CA338273310

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027844-G-T
• MyVariant Identifiers: chr1:g.17354339G>T (hg19) ; chr1:g.17027844G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027844G>T , CM000663.2:g.17027844G>T	GRCh38
NC_000001.10:g.17354339G>T , CM000663.1:g.17354339G>T	GRCh37
NC_000001.9:g.17226926G>T	NCBI36
NG_012340.1:g.31327C>A , LRG_316:g.31327C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.274C>A	ENSP00000481376.2:p.Gln92Lys
ENST00000491274.6:c.403C>A	ENSP00000480482.2:p.Gln135Lys
ENST00000375499.8:c.445C>A MANE Select	ENSP00000364649.3:p.Gln149Lys
ENST00000375499.7:c.445C>A	ENSP00000364649.3:p.Gln149Lys
ENST00000463045.2:c.274C>A	ENSP00000481376.1:p.Gln92Lys
ENST00000475506.1:n.362C>A
ENST00000485515.5:n.379C>A
ENST00000491274.5:c.403C>A	ENSP00000480482.1:p.Gln135Lys
NM_003000.2:c.445C>A , LRG_316t1:c.445C>A	NP_002991.2:p.Gln149Lys
NM_003000.3:c.445C>A MANE Select	NP_002991.2:p.Gln149Lys