Canonical Allele Identifier: CA338228088

Gene: SDHB

Linked Data

• gnomAD v4: 1-17044822-A-G
• MyVariant Identifiers: chr1:g.17371317A>G (hg19) ; chr1:g.17044822A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044822A>G , CM000663.2:g.17044822A>G	GRCh38
NC_000001.10:g.17371317A>G , CM000663.1:g.17371317A>G	GRCh37
NC_000001.9:g.17243904A>G	NCBI36
NG_012340.1:g.14349T>C , LRG_316:g.14349T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-33T>C	ENSP00000481376.2:n.-33T>C
ENST00000491274.6:c.97T>C	ENSP00000480482.2:p.Trp33Arg
ENST00000375499.8:c.139T>C MANE Select	ENSP00000364649.3:p.Trp47Arg
ENST00000375499.7:c.139T>C	ENSP00000364649.3:p.Trp47Arg
ENST00000463045.2:c.-33T>C	ENSP00000481376.1:n.-33T>C
ENST00000466613.2:n.151T>C
ENST00000475506.1:n.56T>C
ENST00000485515.5:n.127T>C
ENST00000491274.5:c.97T>C	ENSP00000480482.1:p.Trp33Arg
NM_003000.2:c.139T>C , LRG_316t1:c.139T>C	NP_002991.2:p.Trp47Arg
NM_003000.3:c.139T>C MANE Select	NP_002991.2:p.Trp47Arg