Canonical Allele Identifier: CA1156077938
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077967398
gnomAD v4: 1-17022549-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022549C>T , CM000663.2:g.17022549C>T GRCh38
NC_000001.10:g.17349044C>T , CM000663.1:g.17349044C>T GRCh37
NC_000001.9:g.17221631C>T NCBI36
NG_012340.1:g.36622G>A , LRG_316:g.36622G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.594+59G>A ENSP00000481376.2:n.594+59G>A
ENST00000491274.6:c.723+59G>A ENSP00000480482.2:n.723+59G>A
ENST00000375499.8:c.765+59G>A MANE Select ENSP00000364649.3:n.765+59G>A
ENST00000375499.7:c.765+59G>A ENSP00000364649.3:n.765+59G>A
ENST00000475049.5:n.190+59G>A
ENST00000485092.5:n.429+59G>A
NM_003000.2:c.765+59G>A , LRG_316t1:c.765+59G>A NP_002991.2:n.765+59G>A
NM_003000.3:c.765+59G>A MANE Select NP_002991.2:n.765+59G>A
Search 100 bp 5'
Search 100 bp 3'