Canonical Allele Identifier: CA18663096

Gene: SDHB

Linked Data

• dbSNP Id: rs200273293
• gnomAD v3: 1-17023924-T-A
• gnomAD v4: 1-17023924-T-A
• MyVariant Identifiers: chr1:g.17350419T>A (hg19) ; chr1:g.17023924T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17023924T>A , CM000663.2:g.17023924T>A	GRCh38
NC_000001.10:g.17350419T>A , CM000663.1:g.17350419T>A	GRCh37
NC_000001.9:g.17223006T>A	NCBI36
NG_012340.1:g.35247A>T , LRG_316:g.35247A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.471+49A>T	ENSP00000481376.2:n.471+49A>T
ENST00000491274.6:c.600+49A>T	ENSP00000480482.2:n.600+49A>T
ENST00000375499.8:c.642+49A>T MANE Select	ENSP00000364649.3:n.642+49A>T
ENST00000375499.7:c.642+49A>T	ENSP00000364649.3:n.642+49A>T
ENST00000485515.5:n.576+49A>T
NM_003000.2:c.642+49A>T , LRG_316t1:c.642+49A>T	NP_002991.2:n.642+49A>T
NM_003000.3:c.642+49A>T MANE Select	NP_002991.2:n.642+49A>T