Canonical Allele Identifier: CA2643675553
Gene: SDHB HGNC NCBI

Linked Data

gnomAD v4: 1-17022529-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022529C>T , CM000663.2:g.17022529C>T GRCh38
NC_000001.10:g.17349024C>T , CM000663.1:g.17349024C>T GRCh37
NC_000001.9:g.17221611C>T NCBI36
NG_012340.1:g.36642G>A , LRG_316:g.36642G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+79G>A ENSP00000481376.2:n.594+79G>A
ENST00000491274.6:c.723+79G>A ENSP00000480482.2:n.723+79G>A
ENST00000375499.8:c.765+79G>A MANE Select ENSP00000364649.3:n.765+79G>A
ENST00000375499.7:c.765+79G>A ENSP00000364649.3:n.765+79G>A
ENST00000475049.5:n.190+79G>A
ENST00000485092.5:n.429+79G>A
NM_003000.2:c.765+79G>A , LRG_316t1:c.765+79G>A NP_002991.2:n.765+79G>A
NM_003000.3:c.765+79G>A MANE Select NP_002991.2:n.765+79G>A