Canonical Allele Identifier: CA2643675862
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs2101514198
gnomAD v4: 1-17022796-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022796T>A , CM000663.2:g.17022796T>A GRCh38
NC_000001.10:g.17349291T>A , CM000663.1:g.17349291T>A GRCh37
NC_000001.9:g.17221878T>A NCBI36
NG_012340.1:g.36375A>T , LRG_316:g.36375A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-66A>T ENSP00000481376.2:n.472-66A>T
ENST00000491274.6:c.601-66A>T ENSP00000480482.2:n.601-66A>T
ENST00000375499.8:c.643-66A>T MANE Select ENSP00000364649.3:n.643-66A>T
ENST00000375499.7:c.643-66A>T ENSP00000364649.3:n.643-66A>T
ENST00000475049.5:n.68-66A>T
ENST00000485092.5:n.241A>T
ENST00000485515.5:n.577-66A>T
NM_003000.2:c.643-66A>T , LRG_316t1:c.643-66A>T NP_002991.2:n.643-66A>T
NM_003000.3:c.643-66A>T MANE Select NP_002991.2:n.643-66A>T