Canonical Allele Identifier: CA338275311
Gene: SDHB HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.17355233T>G (hg19) chr1:g.17028738T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17028738T>G , CM000663.2:g.17028738T>G GRCh38
NC_000001.10:g.17355233T>G , CM000663.1:g.17355233T>G GRCh37
NC_000001.9:g.17227820T>G NCBI36
NG_012340.1:g.30433A>C , LRG_316:g.30433A>C

Transcript Alleles

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