Canonical Allele Identifier: CA18662469
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs985147382
gnomAD v4: 1-17022986-A-G
MyVariant Identifiers: chr1:g.17349481A>G (hg19) chr1:g.17022986A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022986A>G , CM000663.2:g.17022986A>G GRCh38
NC_000001.10:g.17349481A>G , CM000663.1:g.17349481A>G GRCh37
NC_000001.9:g.17222068A>G NCBI36
NG_012340.1:g.36185T>C , LRG_316:g.36185T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.472-256T>C ENSP00000481376.2:n.472-256T>C
ENST00000491274.6:c.601-256T>C ENSP00000480482.2:n.601-256T>C
ENST00000375499.8:c.643-256T>C MANE Select ENSP00000364649.3:n.643-256T>C
ENST00000375499.7:c.643-256T>C ENSP00000364649.3:n.643-256T>C
ENST00000475049.5:n.67+108T>C
ENST00000485092.5:n.51T>C
ENST00000485515.5:n.577-256T>C
NM_003000.2:c.643-256T>C , LRG_316t1:c.643-256T>C NP_002991.2:n.643-256T>C
NM_003000.3:c.643-256T>C MANE Select NP_002991.2:n.643-256T>C
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