Canonical Allele Identifier: CA1980451815

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1327519025

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036222G>T , CM000673.2:g.68036222G>T	GRCh38
NC_000011.9:g.67803689G>T , CM000673.1:g.67803689G>T	GRCh37
NC_000011.8:g.67560265G>T	NCBI36
NG_007878.1:g.2207G>T , LRG_115:g.2207G>T
NG_017040.1:g.10606G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.373-31G>T MANE Select	ENSP00000315774.5:n.373-31G>T
ENST00000313468.9:c.373-31G>T	ENSP00000315774.5:n.373-31G>T
ENST00000524810.5:c.305-31G>T
ENST00000525419.5:c.319-31G>T	ENSP00000433521.1:n.319-31G>T
ENST00000526339.5:c.373-31G>T	ENSP00000436287.1:n.373-31G>T
ENST00000526446.5:c.*428-31G>T	ENSP00000433645.1:n.*428-31G>T
ENST00000526542.1:n.324-31G>T
ENST00000528492.1:c.-66-31G>T	ENSP00000432848.1:n.-66-31G>T
ENST00000531282.1:n.194G>T
NM_002496.3:c.373-31G>T	NP_002487.1:n.373-31G>T
XM_005274013.1:c.373-31G>T	XP_005274070.1:n.373-31G>T
XM_005274014.1:c.373-31G>T	XP_005274071.1:n.373-31G>T
XM_005274015.1:c.253-31G>T	XP_005274072.1:n.253-31G>T
XM_011545053.1:c.373-31G>T	XP_011543355.1:n.373-31G>T
NM_002496.4:c.373-31G>T MANE Select	NP_002487.1:n.373-31G>T