Canonical Allele Identifier: CA338270056

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349124G>T (hg19) ; chr1:g.17022629G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17022629G>T , CM000663.2:g.17022629G>T	GRCh38
NC_000001.10:g.17349124G>T , CM000663.1:g.17349124G>T	GRCh37
NC_000001.9:g.17221711G>T	NCBI36
NG_012340.1:g.36542C>A , LRG_316:g.36542C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.573C>A	ENSP00000481376.2:p.Asn191Lys
ENST00000491274.6:c.702C>A	ENSP00000480482.2:p.Asn234Lys
ENST00000375499.8:c.744C>A MANE Select	ENSP00000364649.3:p.Asn248Lys
ENST00000375499.7:c.744C>A	ENSP00000364649.3:p.Asn248Lys
ENST00000475049.5:n.169C>A
ENST00000485092.5:n.408C>A
ENST00000485515.5:n.678C>A
NM_003000.2:c.744C>A , LRG_316t1:c.744C>A	NP_002991.2:p.Asn248Lys
NM_003000.3:c.744C>A MANE Select	NP_002991.2:p.Asn248Lys