Canonical Allele Identifier: CA222882655

Gene: SDHAF2

Linked Data

• dbSNP Id: rs909359675
• MyVariant Identifiers: chr11:g.61213613T>C (hg19) ; chr11:g.61446141T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61446141T>C , CM000673.2:g.61446141T>C	GRCh38
NC_000011.9:g.61213613T>C , CM000673.1:g.61213613T>C	GRCh37
NC_000011.8:g.60970189T>C	NCBI36
NG_023393.1:g.21017T>C , LRG_519:g.21017T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301761.7:c.*70T>C MANE Select	ENSP00000301761.3:n.*70T>C
ENST00000301761.6:c.*70T>C	ENSP00000301761.2:n.*70T>C
ENST00000536670.5:n.396+8028T>C
ENST00000538594.5:c.370+8028T>C	ENSP00000440939.1:n.370+8028T>C
ENST00000541135.5:c.377+8021T>C	ENSP00000443130.1:n.377+8021T>C
ENST00000542074.1:c.*150T>C	ENSP00000469670.1:n.*150T>C
ENST00000542794.5:c.*573T>C	ENSP00000439983.1:n.*573T>C
ENST00000543044.2:c.*70T>C	ENSP00000440219.1:n.*70T>C
ENST00000544025.5:n.465+8028T>C
ENST00000544801.5:c.370+8028T>C	ENSP00000442581.1:n.370+8028T>C
ENST00000544880.1:n.374+8028T>C
NM_017841.2:c.*70T>C , LRG_519t1:c.*70T>C	NP_060311.1:n.*70T>C
NM_017841.4:c.*70T>C MANE Select	NP_060311.1:n.*70T>C