Canonical Allele Identifier: CA18665685
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs985398510
gnomAD v2: 1-17354096-G-A
gnomAD v3: 1-17027601-G-A
gnomAD v4: 1-17027601-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17027601G>A , CM000663.2:g.17027601G>A GRCh38
NC_000001.10:g.17354096G>A , CM000663.1:g.17354096G>A GRCh37
NC_000001.9:g.17226683G>A NCBI36
NG_012340.1:g.31570C>T , LRG_316:g.31570C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.369+148C>T ENSP00000481376.2:n.369+148C>T
ENST00000491274.6:c.498+148C>T ENSP00000480482.2:n.498+148C>T
ENST00000375499.8:c.540+148C>T MANE Select ENSP00000364649.3:n.540+148C>T
ENST00000375499.7:c.540+148C>T ENSP00000364649.3:n.540+148C>T
ENST00000485515.5:n.474+148C>T
ENST00000491274.5:c.498+148C>T ENSP00000480482.1:n.498+148C>T
NM_003000.2:c.540+148C>T , LRG_316t1:c.540+148C>T NP_002991.2:n.540+148C>T
NM_003000.3:c.540+148C>T MANE Select NP_002991.2:n.540+148C>T