Canonical Allele Identifier: CA338275131

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355219G>T (hg19) ; chr1:g.17028724G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028724G>T , CM000663.2:g.17028724G>T	GRCh38
NC_000001.10:g.17355219G>T , CM000663.1:g.17355219G>T	GRCh37
NC_000001.9:g.17227806G>T	NCBI36
NG_012340.1:g.30447C>A , LRG_316:g.30447C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.128C>A	ENSP00000481376.2:p.Ser43Tyr
ENST00000491274.6:c.257C>A	ENSP00000480482.2:p.Ser86Tyr
ENST00000375499.8:c.299C>A MANE Select	ENSP00000364649.3:p.Ser100Tyr
ENST00000375499.7:c.299C>A	ENSP00000364649.3:p.Ser100Tyr
ENST00000463045.2:c.128C>A	ENSP00000481376.1:p.Ser43Tyr
ENST00000475506.1:n.216C>A
ENST00000485515.5:n.287C>A
ENST00000491274.5:c.257C>A	ENSP00000480482.1:p.Ser86Tyr
NM_003000.2:c.299C>A , LRG_316t1:c.299C>A	NP_002991.2:p.Ser100Tyr
NM_003000.3:c.299C>A MANE Select	NP_002991.2:p.Ser100Tyr