Canonical Allele Identifier: CA338270466

Gene: SDHB

Linked Data

• dbSNP Id: rs2101513961
• MyVariant Identifiers: chr1:g.17349206T>A (hg19) ; chr1:g.17022711T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022711T>A , CM000663.2:g.17022711T>A	GRCh38
NC_000001.10:g.17349206T>A , CM000663.1:g.17349206T>A	GRCh37
NC_000001.9:g.17221793T>A	NCBI36
NG_012340.1:g.36460A>T , LRG_316:g.36460A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.491A>T	ENSP00000481376.2:p.Asp164Val
ENST00000491274.6:c.620A>T	ENSP00000480482.2:p.Asp207Val
ENST00000375499.8:c.662A>T MANE Select	ENSP00000364649.3:p.Asp221Val
ENST00000375499.7:c.662A>T	ENSP00000364649.3:p.Asp221Val
ENST00000475049.5:n.87A>T
ENST00000485092.5:n.326A>T
ENST00000485515.5:n.596A>T
NM_003000.2:c.662A>T , LRG_316t1:c.662A>T	NP_002991.2:p.Asp221Val
NM_003000.3:c.662A>T MANE Select	NP_002991.2:p.Asp221Val