Canonical Allele Identifier: CA2613847671

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446277-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446277T>C , CM000673.2:g.61446277T>C	GRCh38
NC_000011.9:g.61213749T>C , CM000673.1:g.61213749T>C	GRCh37
NC_000011.8:g.60970325T>C	NCBI36
NG_023393.1:g.21153T>C , LRG_519:g.21153T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*206T>C MANE Select	ENSP00000301761.3:n.*206T>C
ENST00000301761.6:c.*206T>C	ENSP00000301761.2:n.*206T>C
ENST00000536670.5:n.396+8164T>C
ENST00000538594.5:c.370+8164T>C	ENSP00000440939.1:n.370+8164T>C
ENST00000541135.5:c.377+8157T>C	ENSP00000443130.1:n.377+8157T>C
ENST00000542074.1:c.*286T>C	ENSP00000469670.1:n.*286T>C
ENST00000542794.5:c.*709T>C	ENSP00000439983.1:n.*709T>C
ENST00000543044.2:c.*160+46T>C	ENSP00000440219.1:n.*160+46T>C
ENST00000544025.5:n.465+8164T>C
ENST00000544801.5:c.370+8164T>C	ENSP00000442581.1:n.370+8164T>C
ENST00000544880.1:n.374+8164T>C
NM_017841.2:c.*206T>C , LRG_519t1:c.*206T>C	NP_060311.1:n.*206T>C
NM_017841.4:c.*206T>C MANE Select	NP_060311.1:n.*206T>C