Canonical Allele Identifier: CA1156078101
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2077970011

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022902dup , CM000663.2:g.17022902dup GRCh38
NC_000001.10:g.17349397dup , CM000663.1:g.17349397dup GRCh37
NC_000001.9:g.17221984dup NCBI36
NG_012340.1:g.36269dup , LRG_316:g.36269dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-172dup ENSP00000481376.2:n.472-172dup
ENST00000491274.6:c.601-172dup ENSP00000480482.2:n.601-172dup
ENST00000375499.8:c.643-172dup MANE Select ENSP00000364649.3:n.643-172dup
ENST00000375499.7:c.643-172dup ENSP00000364649.3:n.643-172dup
ENST00000475049.5:n.68-172dup
ENST00000485092.5:n.135dup
ENST00000485515.5:n.577-172dup
NM_003000.2:c.643-172dup , LRG_316t1:c.643-172dup NP_002991.2:n.643-172dup
NM_003000.3:c.643-172dup MANE Select NP_002991.2:n.643-172dup