Canonical Allele Identifier: CA338227989

Gene: SDHB

Linked Data

• gnomAD v4: 1-17044812-T-G
• MyVariant Identifiers: chr1:g.17371307T>G (hg19) ; chr1:g.17044812T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044812T>G , CM000663.2:g.17044812T>G	GRCh38
NC_000001.10:g.17371307T>G , CM000663.1:g.17371307T>G	GRCh37
NC_000001.9:g.17243894T>G	NCBI36
NG_012340.1:g.14359A>C , LRG_316:g.14359A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-23A>C	ENSP00000481376.2:n.-23A>C
ENST00000491274.6:c.107A>C	ENSP00000480482.2:p.Asp36Ala
ENST00000375499.8:c.149A>C MANE Select	ENSP00000364649.3:p.Asp50Ala
ENST00000375499.7:c.149A>C	ENSP00000364649.3:p.Asp50Ala
ENST00000463045.2:c.-23A>C	ENSP00000481376.1:n.-23A>C
ENST00000466613.2:n.161A>C
ENST00000475506.1:n.66A>C
ENST00000485515.5:n.137A>C
ENST00000491274.5:c.107A>C	ENSP00000480482.1:p.Asp36Ala
NM_003000.2:c.149A>C , LRG_316t1:c.149A>C	NP_002991.2:p.Asp50Ala
NM_003000.3:c.149A>C MANE Select	NP_002991.2:p.Asp50Ala