Canonical Allele Identifier: CA416081774

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17349124G>A (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000463045.3:c.573C>T	ENSP00000481376.2:p.Asn191=
ENST00000491274.6:c.702C>T	ENSP00000480482.2:p.Asn234=
ENST00000375499.8:c.744C>T MANE Select	ENSP00000364649.3:p.Asn248=
ENST00000375499.7:c.744C>T	ENSP00000364649.3:p.Asn248=
ENST00000475049.5:n.169C>T
ENST00000485092.5:n.408C>T
ENST00000485515.5:n.678C>T
NM_003000.2:c.744C>T , LRG_316t1:c.744C>T	NP_002991.2:p.Asn248=
NM_003000.3:c.744C>T MANE Select	NP_002991.2:p.Asn248=