Canonical Allele Identifier: CA1977301489
Gene: SDHAF2 HGNC NCBI

Linked Data

dbSNP Id: rs1862139067

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446407G>A , CM000673.2:g.61446407G>A GRCh38
NC_000011.9:g.61213879G>A , CM000673.1:g.61213879G>A GRCh37
NC_000011.8:g.60970455G>A NCBI36
NG_023393.1:g.21283G>A , LRG_519:g.21283G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*336G>A MANE Select ENSP00000301761.3:n.*336G>A
ENST00000301761.6:c.*336G>A ENSP00000301761.2:n.*336G>A
ENST00000536670.5:n.396+8294G>A
ENST00000538594.5:c.370+8294G>A ENSP00000440939.1:n.370+8294G>A
ENST00000541135.5:c.377+8287G>A ENSP00000443130.1:n.377+8287G>A
ENST00000542074.1:c.*416G>A ENSP00000469670.1:n.*416G>A
ENST00000543044.2:c.*160+176G>A ENSP00000440219.1:n.*160+176G>A
ENST00000544025.5:n.465+8294G>A
ENST00000544801.5:c.370+8294G>A ENSP00000442581.1:n.370+8294G>A
ENST00000544880.1:n.374+8294G>A
NM_017841.2:c.*336G>A , LRG_519t1:c.*336G>A NP_060311.1:n.*336G>A
NM_017841.4:c.*336G>A MANE Select NP_060311.1:n.*336G>A