Canonical Allele Identifier: CA1977301601
Gene: SDHAF2 HGNC NCBI

Linked Data

dbSNP Id: rs1590769626

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446497G>A , CM000673.2:g.61446497G>A GRCh38
NC_000011.9:g.61213969G>A , CM000673.1:g.61213969G>A GRCh37
NC_000011.8:g.60970545G>A NCBI36
NG_023393.1:g.21373G>A , LRG_519:g.21373G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*426G>A MANE Select ENSP00000301761.3:n.*426G>A
ENST00000301761.6:c.*426G>A ENSP00000301761.2:n.*426G>A
ENST00000536670.5:n.396+8384G>A
ENST00000538594.5:c.370+8384G>A ENSP00000440939.1:n.370+8384G>A
ENST00000541135.5:c.377+8377G>A ENSP00000443130.1:n.377+8377G>A
ENST00000542074.1:c.*506G>A ENSP00000469670.1:n.*506G>A
ENST00000543044.2:c.*160+266G>A ENSP00000440219.1:n.*160+266G>A
ENST00000544025.5:n.465+8384G>A
ENST00000544801.5:c.370+8384G>A ENSP00000442581.1:n.370+8384G>A
ENST00000544880.1:n.374+8384G>A
NM_017841.2:c.*426G>A , LRG_519t1:c.*426G>A NP_060311.1:n.*426G>A
NM_017841.4:c.*426G>A MANE Select NP_060311.1:n.*426G>A