Canonical Allele Identifier: CA2613847600
Gene: SDHAF2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446238G>T , CM000673.2:g.61446238G>T GRCh38
NC_000011.9:g.61213710G>T , CM000673.1:g.61213710G>T GRCh37
NC_000011.8:g.60970286G>T NCBI36
NG_023393.1:g.21114G>T , LRG_519:g.21114G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*167G>T MANE Select ENSP00000301761.3:n.*167G>T
ENST00000301761.6:c.*167G>T ENSP00000301761.2:n.*167G>T
ENST00000536670.5:n.396+8125G>T
ENST00000538594.5:c.370+8125G>T ENSP00000440939.1:n.370+8125G>T
ENST00000541135.5:c.377+8118G>T ENSP00000443130.1:n.377+8118G>T
ENST00000542074.1:c.*247G>T ENSP00000469670.1:n.*247G>T
ENST00000542794.5:c.*670G>T ENSP00000439983.1:n.*670G>T
ENST00000543044.2:c.*160+7G>T ENSP00000440219.1:n.*160+7G>T
ENST00000544025.5:n.465+8125G>T
ENST00000544801.5:c.370+8125G>T ENSP00000442581.1:n.370+8125G>T
ENST00000544880.1:n.374+8125G>T
NM_017841.2:c.*167G>T , LRG_519t1:c.*167G>T NP_060311.1:n.*167G>T
NM_017841.4:c.*167G>T MANE Select NP_060311.1:n.*167G>T