Canonical Allele Identifier: CA381570544
Gene: NDUFS8 HGNC NCBI

Linked Data

dbSNP Id: rs569695304

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.68036589G>T , CM000673.2:g.68036589G>T GRCh38
NC_000011.9:g.67804056G>T , CM000673.1:g.67804056G>T GRCh37
NC_000011.8:g.67560632G>T NCBI36
NG_007878.1:g.2574G>T , LRG_115:g.2574G>T
NG_017040.1:g.10973G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313468.10:c.629G>T MANE Select ENSP00000315774.5:p.Arg210Leu
ENST00000313468.9:c.629G>T ENSP00000315774.5:p.Arg210Leu
ENST00000524810.5:c.561G>T
ENST00000528492.1:c.191G>T ENSP00000432848.1:p.Arg64Leu
ENST00000531282.1:n.481G>T
NM_002496.3:c.629G>T NP_002487.1:p.Arg210Leu
XM_005274013.1:c.629G>T XP_005274070.1:p.Arg210Leu
XM_005274014.1:c.629G>T XP_005274071.1:p.Arg210Leu
XM_005274015.1:c.509G>T XP_005274072.1:p.Arg170Leu
XM_011545053.1:c.629G>T XP_011543355.1:p.Arg210Leu
NM_002496.4:c.629G>T MANE Select NP_002487.1:p.Arg210Leu