Canonical Allele Identifier: CA2643678089
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1553177772
gnomAD v4: 1-17028739-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028739G>A , CM000663.2:g.17028739G>A GRCh38
NC_000001.10:g.17355234G>A , CM000663.1:g.17355234G>A GRCh37
NC_000001.9:g.17227821G>A NCBI36
NG_012340.1:g.30432C>T , LRG_316:g.30432C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000463045.3:c.116-3C>T ENSP00000481376.2:n.116-3C>T
ENST00000491274.6:c.245-3C>T ENSP00000480482.2:n.245-3C>T
ENST00000375499.8:c.287-3C>T MANE Select ENSP00000364649.3:n.287-3C>T
ENST00000375499.7:c.287-3C>T ENSP00000364649.3:n.287-3C>T
ENST00000463045.2:c.116-3C>T ENSP00000481376.1:n.116-3C>T
ENST00000475506.1:n.204-3C>T
ENST00000485515.5:n.275-3C>T
ENST00000491274.5:c.245-3C>T ENSP00000480482.1:n.245-3C>T
NM_003000.2:c.287-3C>T , LRG_316t1:c.287-3C>T NP_002991.2:n.287-3C>T
NM_003000.3:c.287-3C>T MANE Select NP_002991.2:n.287-3C>T