Canonical Allele Identifier: CA338275113

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17355216C>A (hg19) ; chr1:g.17028721C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17028721C>A , CM000663.2:g.17028721C>A	GRCh38
NC_000001.10:g.17355216C>A , CM000663.1:g.17355216C>A	GRCh37
NC_000001.9:g.17227803C>A	NCBI36
NG_012340.1:g.30450G>T , LRG_316:g.30450G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.131G>T	ENSP00000481376.2:p.Cys44Phe
ENST00000491274.6:c.260G>T	ENSP00000480482.2:p.Cys87Phe
ENST00000375499.8:c.302G>T MANE Select	ENSP00000364649.3:p.Cys101Phe
ENST00000375499.7:c.302G>T	ENSP00000364649.3:p.Cys101Phe
ENST00000463045.2:c.131G>T	ENSP00000481376.1:p.Cys44Phe
ENST00000475506.1:n.219G>T
ENST00000485515.5:n.290G>T
ENST00000491274.5:c.260G>T	ENSP00000480482.1:p.Cys87Phe
NM_003000.2:c.302G>T , LRG_316t1:c.302G>T	NP_002991.2:p.Cys101Phe
NM_003000.3:c.302G>T MANE Select	NP_002991.2:p.Cys101Phe