Canonical Allele Identifier: CA1156080102

Gene: SDHB

Linked Data

• dbSNP Id: rs999493734
• gnomAD v4: 1-17027618-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027618C>A , CM000663.2:g.17027618C>A	GRCh38
NC_000001.10:g.17354113C>A , CM000663.1:g.17354113C>A	GRCh37
NC_000001.9:g.17226700C>A	NCBI36
NG_012340.1:g.31553G>T , LRG_316:g.31553G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.369+131G>T	ENSP00000481376.2:n.369+131G>T
ENST00000491274.6:c.498+131G>T	ENSP00000480482.2:n.498+131G>T
ENST00000375499.8:c.540+131G>T MANE Select	ENSP00000364649.3:n.540+131G>T
ENST00000375499.7:c.540+131G>T	ENSP00000364649.3:n.540+131G>T
ENST00000485515.5:n.474+131G>T
ENST00000491274.5:c.498+131G>T	ENSP00000480482.1:n.498+131G>T
NM_003000.2:c.540+131G>T , LRG_316t1:c.540+131G>T	NP_002991.2:n.540+131G>T
NM_003000.3:c.540+131G>T MANE Select	NP_002991.2:n.540+131G>T