Canonical Allele Identifier: CA2724396604

Gene: NDUFS8

Linked Data

• dbSNP Id: rs2134414206

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68033040A>C , CM000673.2:g.68033040A>C	GRCh38
NC_000011.9:g.67800507A>C , CM000673.1:g.67800507A>C	GRCh37
NC_000011.8:g.67557083A>C	NCBI36
NG_017040.1:g.7424A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.199+28A>C MANE Select	ENSP00000315774.5:n.199+28A>C
ENST00000313468.9:c.199+28A>C	ENSP00000315774.5:n.199+28A>C
ENST00000432321.6:n.316+28A>C
ENST00000453471.6:c.199+28A>C	ENSP00000403972.2:n.199+28A>C
ENST00000525419.5:c.145+28A>C	ENSP00000433521.1:n.145+28A>C
ENST00000525628.1:c.199+28A>C	ENSP00000432968.1:n.199+28A>C
ENST00000526339.5:c.199+28A>C	ENSP00000436287.1:n.199+28A>C
ENST00000526446.5:c.*254+28A>C	ENSP00000433645.1:n.*254+28A>C
ENST00000528492.1:c.-67+2307A>C	ENSP00000432848.1:n.-67+2307A>C
ENST00000529645.1:c.377+28A>C	ENSP00000431293.1:n.377+28A>C
ENST00000531228.1:c.*41+28A>C	ENSP00000433054.1:n.*41+28A>C
ENST00000532399.1:n.834A>C
NM_002496.3:c.199+28A>C	NP_002487.1:n.199+28A>C
XM_005274013.1:c.199+28A>C	XP_005274070.1:n.199+28A>C
XM_005274014.1:c.199+28A>C	XP_005274071.1:n.199+28A>C
XM_005274015.1:c.79+28A>C	XP_005274072.1:n.79+28A>C
XM_011545053.1:c.199+28A>C	XP_011543355.1:n.199+28A>C
NM_002496.4:c.199+28A>C MANE Select	NP_002487.1:n.199+28A>C