Canonical Allele Identifier: CA890984682

Gene: SDHB

Linked Data

• dbSNP Id: rs1261901107
• gnomAD v3: 1-17022169-G-A
• gnomAD v4: 1-17022169-G-A
• MyVariant Identifiers: chr1:g.17348664G>A (hg19) ; chr1:g.17022169G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022169G>A , CM000663.2:g.17022169G>A	GRCh38
NC_000001.10:g.17348664G>A , CM000663.1:g.17348664G>A	GRCh37
NC_000001.9:g.17221251G>A	NCBI36
NG_012340.1:g.37002C>T , LRG_316:g.37002C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.594+439C>T	ENSP00000481376.2:n.594+439C>T
ENST00000491274.6:c.723+439C>T	ENSP00000480482.2:n.723+439C>T
ENST00000375499.8:c.765+439C>T MANE Select	ENSP00000364649.3:n.765+439C>T
ENST00000375499.7:c.765+439C>T	ENSP00000364649.3:n.765+439C>T
ENST00000475049.5:n.190+439C>T
ENST00000485092.5:n.429+439C>T
NM_003000.2:c.765+439C>T , LRG_316t1:c.765+439C>T	NP_002991.2:n.765+439C>T
NM_003000.3:c.765+439C>T MANE Select	NP_002991.2:n.765+439C>T