Canonical Allele Identifier: CA2723708992
Gene: SDHAF2 HGNC NCBI

Linked Data

dbSNP Id: rs937752231

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61446461G>C , CM000673.2:g.61446461G>C GRCh38
NC_000011.9:g.61213933G>C , CM000673.1:g.61213933G>C GRCh37
NC_000011.8:g.60970509G>C NCBI36
NG_023393.1:g.21337G>C , LRG_519:g.21337G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301761.7:c.*390G>C MANE Select ENSP00000301761.3:n.*390G>C
ENST00000301761.6:c.*390G>C ENSP00000301761.2:n.*390G>C
ENST00000536670.5:n.396+8348G>C
ENST00000538594.5:c.370+8348G>C ENSP00000440939.1:n.370+8348G>C
ENST00000541135.5:c.377+8341G>C ENSP00000443130.1:n.377+8341G>C
ENST00000542074.1:c.*470G>C ENSP00000469670.1:n.*470G>C
ENST00000543044.2:c.*160+230G>C ENSP00000440219.1:n.*160+230G>C
ENST00000544025.5:n.465+8348G>C
ENST00000544801.5:c.370+8348G>C ENSP00000442581.1:n.370+8348G>C
ENST00000544880.1:n.374+8348G>C
NM_017841.2:c.*390G>C , LRG_519t1:c.*390G>C NP_060311.1:n.*390G>C
NM_017841.4:c.*390G>C MANE Select NP_060311.1:n.*390G>C