Canonical Allele Identifier: CA381570482

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67804052T>C (hg19) ; chr11:g.68036585T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036585T>C , CM000673.2:g.68036585T>C	GRCh38
NC_000011.9:g.67804052T>C , CM000673.1:g.67804052T>C	GRCh37
NC_000011.8:g.67560628T>C	NCBI36
NG_007878.1:g.2570T>C , LRG_115:g.2570T>C
NG_017040.1:g.10969T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.625T>C MANE Select	ENSP00000315774.5:p.Tyr209His
ENST00000313468.9:c.625T>C	ENSP00000315774.5:p.Tyr209His
ENST00000524810.5:c.557T>C
ENST00000528492.1:c.187T>C	ENSP00000432848.1:p.Tyr63His
ENST00000531282.1:n.477T>C
NM_002496.3:c.625T>C	NP_002487.1:p.Tyr209His
XM_005274013.1:c.625T>C	XP_005274070.1:p.Tyr209His
XM_005274014.1:c.625T>C	XP_005274071.1:p.Tyr209His
XM_005274015.1:c.505T>C	XP_005274072.1:p.Tyr169His
XM_011545053.1:c.625T>C	XP_011543355.1:p.Tyr209His
NM_002496.4:c.625T>C MANE Select	NP_002487.1:p.Tyr209His