Canonical Allele Identifier: CA18662471
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs909120487
gnomAD v3: 1-17022993-C-T
gnomAD v4: 1-17022993-C-T
MyVariant Identifiers: chr1:g.17349488C>T (hg19) chr1:g.17022993C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022993C>T , CM000663.2:g.17022993C>T GRCh38
NC_000001.10:g.17349488C>T , CM000663.1:g.17349488C>T GRCh37
NC_000001.9:g.17222075C>T NCBI36
NG_012340.1:g.36178G>A , LRG_316:g.36178G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-263G>A ENSP00000481376.2:n.472-263G>A
ENST00000491274.6:c.601-263G>A ENSP00000480482.2:n.601-263G>A
ENST00000375499.8:c.643-263G>A MANE Select ENSP00000364649.3:n.643-263G>A
ENST00000375499.7:c.643-263G>A ENSP00000364649.3:n.643-263G>A
ENST00000475049.5:n.67+101G>A
ENST00000485092.5:n.44G>A
ENST00000485515.5:n.577-263G>A
NM_003000.2:c.643-263G>A , LRG_316t1:c.643-263G>A NP_002991.2:n.643-263G>A
NM_003000.3:c.643-263G>A MANE Select NP_002991.2:n.643-263G>A
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