Canonical Allele Identifier: CA338227977

Gene: SDHB

Linked Data

• ClinVar Variation Id: 1427491
• ClinVar RCV Id: RCV001945934
• dbSNP Id: rs2101541430
• MyVariant Identifiers: chr1:g.17371304T>G (hg19) ; chr1:g.17044809T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17044809T>G , CM000663.2:g.17044809T>G	GRCh38
NC_000001.10:g.17371304T>G , CM000663.1:g.17371304T>G	GRCh37
NC_000001.9:g.17243891T>G	NCBI36
NG_012340.1:g.14362A>C , LRG_316:g.14362A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.-20A>C	ENSP00000481376.2:n.-20A>C
ENST00000491274.6:c.110A>C	ENSP00000480482.2:p.Lys37Thr
ENST00000375499.8:c.152A>C MANE Select	ENSP00000364649.3:p.Lys51Thr
ENST00000375499.7:c.152A>C	ENSP00000364649.3:p.Lys51Thr
ENST00000463045.2:c.-20A>C	ENSP00000481376.1:n.-20A>C
ENST00000466613.2:n.164A>C
ENST00000475506.1:n.69A>C
ENST00000485515.5:n.140A>C
ENST00000491274.5:c.110A>C	ENSP00000480482.1:p.Lys37Thr
NM_003000.2:c.152A>C , LRG_316t1:c.152A>C	NP_002991.2:p.Lys51Thr
NM_003000.3:c.152A>C MANE Select	NP_002991.2:p.Lys51Thr