Canonical Allele Identifier: CA521037385
Gene: SDHB HGNC NCBI

Linked Data

dbSNP Id: rs1388694864
gnomAD v2: 1-17348739-C-T
MyVariant Identifiers: chr1:g.17348739C>T (hg19) chr1:g.17022244C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.17022244C>T , CM000663.2:g.17022244C>T GRCh38
NC_000001.10:g.17348739C>T , CM000663.1:g.17348739C>T GRCh37
NC_000001.9:g.17221326C>T NCBI36
NG_012340.1:g.36927G>A , LRG_316:g.36927G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000463045.3:c.594+364G>A ENSP00000481376.2:n.594+364G>A
ENST00000491274.6:c.723+364G>A ENSP00000480482.2:n.723+364G>A
ENST00000375499.8:c.765+364G>A MANE Select ENSP00000364649.3:n.765+364G>A
ENST00000375499.7:c.765+364G>A ENSP00000364649.3:n.765+364G>A
ENST00000475049.5:n.190+364G>A
ENST00000485092.5:n.429+364G>A
NM_003000.2:c.765+364G>A , LRG_316t1:c.765+364G>A NP_002991.2:n.765+364G>A
NM_003000.3:c.765+364G>A MANE Select NP_002991.2:n.765+364G>A
Search 100 bp 5'
Search 100 bp 3'