Canonical Allele Identifier: CA1977301448

Gene: SDHAF2

Linked Data

• dbSNP Id: rs1862138402
• gnomAD v4: 11-61446362-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446362G>T , CM000673.2:g.61446362G>T	GRCh38
NC_000011.9:g.61213834G>T , CM000673.1:g.61213834G>T	GRCh37
NC_000011.8:g.60970410G>T	NCBI36
NG_023393.1:g.21238G>T , LRG_519:g.21238G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*291G>T MANE Select	ENSP00000301761.3:n.*291G>T
ENST00000301761.6:c.*291G>T	ENSP00000301761.2:n.*291G>T
ENST00000536670.5:n.396+8249G>T
ENST00000538594.5:c.370+8249G>T	ENSP00000440939.1:n.370+8249G>T
ENST00000541135.5:c.377+8242G>T	ENSP00000443130.1:n.377+8242G>T
ENST00000542074.1:c.*371G>T	ENSP00000469670.1:n.*371G>T
ENST00000543044.2:c.*160+131G>T	ENSP00000440219.1:n.*160+131G>T
ENST00000544025.5:n.465+8249G>T
ENST00000544801.5:c.370+8249G>T	ENSP00000442581.1:n.370+8249G>T
ENST00000544880.1:n.374+8249G>T
NM_017841.2:c.*291G>T , LRG_519t1:c.*291G>T	NP_060311.1:n.*291G>T
NM_017841.4:c.*291G>T MANE Select	NP_060311.1:n.*291G>T