Canonical Allele Identifier: CA416085824

Gene: SDHB

Linked Data

• MyVariant Identifiers: chr1:g.17354271C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027776C>A , CM000663.2:g.17027776C>A	GRCh38
NC_000001.10:g.17354271C>A , CM000663.1:g.17354271C>A	GRCh37
NC_000001.9:g.17226858C>A	NCBI36
NG_012340.1:g.31395G>T , LRG_316:g.31395G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.342G>T	ENSP00000481376.2:p.Leu114=
ENST00000491274.6:c.471G>T	ENSP00000480482.2:p.Leu157=
ENST00000375499.8:c.513G>T MANE Select	ENSP00000364649.3:p.Leu171=
ENST00000375499.7:c.513G>T	ENSP00000364649.3:p.Leu171=
ENST00000463045.2:c.342G>T	ENSP00000481376.1:p.Leu114=
ENST00000475506.1:n.430G>T
ENST00000485515.5:n.447G>T
ENST00000491274.5:c.471G>T	ENSP00000480482.1:p.Leu157=
NM_003000.2:c.513G>T , LRG_316t1:c.513G>T	NP_002991.2:p.Leu171=
NM_003000.3:c.513G>T MANE Select	NP_002991.2:p.Leu171=