Canonical Allele Identifier: CA416086378

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027857-G-A
• MyVariant Identifiers: chr1:g.17354352G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027857G>A , CM000663.2:g.17027857G>A	GRCh38
NC_000001.10:g.17354352G>A , CM000663.1:g.17354352G>A	GRCh37
NC_000001.9:g.17226939G>A	NCBI36
NG_012340.1:g.31314C>T , LRG_316:g.31314C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.261C>T	ENSP00000481376.2:p.Ser87=
ENST00000491274.6:c.390C>T	ENSP00000480482.2:p.Ser130=
ENST00000375499.8:c.432C>T MANE Select	ENSP00000364649.3:p.Ser144=
ENST00000375499.7:c.432C>T	ENSP00000364649.3:p.Ser144=
ENST00000463045.2:c.261C>T	ENSP00000481376.1:p.Ser87=
ENST00000475506.1:n.349C>T
ENST00000485515.5:n.366C>T
ENST00000491274.5:c.390C>T	ENSP00000480482.1:p.Ser130=
NM_003000.2:c.432C>T , LRG_316t1:c.432C>T	NP_002991.2:p.Ser144=
NM_003000.3:c.432C>T MANE Select	NP_002991.2:p.Ser144=