Canonical Allele Identifier: CA2613847632

Gene: SDHAF2

Linked Data

• gnomAD v4: 11-61446256-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446256T>C , CM000673.2:g.61446256T>C	GRCh38
NC_000011.9:g.61213728T>C , CM000673.1:g.61213728T>C	GRCh37
NC_000011.8:g.60970304T>C	NCBI36
NG_023393.1:g.21132T>C , LRG_519:g.21132T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*185T>C MANE Select	ENSP00000301761.3:n.*185T>C
ENST00000301761.6:c.*185T>C	ENSP00000301761.2:n.*185T>C
ENST00000536670.5:n.396+8143T>C
ENST00000538594.5:c.370+8143T>C	ENSP00000440939.1:n.370+8143T>C
ENST00000541135.5:c.377+8136T>C	ENSP00000443130.1:n.377+8136T>C
ENST00000542074.1:c.*265T>C	ENSP00000469670.1:n.*265T>C
ENST00000542794.5:c.*688T>C	ENSP00000439983.1:n.*688T>C
ENST00000543044.2:c.*160+25T>C	ENSP00000440219.1:n.*160+25T>C
ENST00000544025.5:n.465+8143T>C
ENST00000544801.5:c.370+8143T>C	ENSP00000442581.1:n.370+8143T>C
ENST00000544880.1:n.374+8143T>C
NM_017841.2:c.*185T>C , LRG_519t1:c.*185T>C	NP_060311.1:n.*185T>C
NM_017841.4:c.*185T>C MANE Select	NP_060311.1:n.*185T>C