Canonical Allele Identifier: CA338273497

Gene: SDHB

Linked Data

• gnomAD v4: 1-17027860-C-A
• MyVariant Identifiers: chr1:g.17354355C>A (hg19) ; chr1:g.17027860C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.17027860C>A , CM000663.2:g.17027860C>A	GRCh38
NC_000001.10:g.17354355C>A , CM000663.1:g.17354355C>A	GRCh37
NC_000001.9:g.17226942C>A	NCBI36
NG_012340.1:g.31311G>T , LRG_316:g.31311G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000463045.3:c.258G>T	ENSP00000481376.2:p.Leu86Phe
ENST00000491274.6:c.387G>T	ENSP00000480482.2:p.Leu129Phe
ENST00000375499.8:c.429G>T MANE Select	ENSP00000364649.3:p.Leu143Phe
ENST00000375499.7:c.429G>T	ENSP00000364649.3:p.Leu143Phe
ENST00000463045.2:c.258G>T	ENSP00000481376.1:p.Leu86Phe
ENST00000475506.1:n.346G>T
ENST00000485515.5:n.363G>T
ENST00000491274.5:c.387G>T	ENSP00000480482.1:p.Leu129Phe
NM_003000.2:c.429G>T , LRG_316t1:c.429G>T	NP_002991.2:p.Leu143Phe
NM_003000.3:c.429G>T MANE Select	NP_002991.2:p.Leu143Phe