Canonical Allele Identifier: CA381568618

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67803719G>C (hg19) ; chr11:g.68036252G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036252G>C , CM000673.2:g.68036252G>C	GRCh38
NC_000011.9:g.67803719G>C , CM000673.1:g.67803719G>C	GRCh37
NC_000011.8:g.67560295G>C	NCBI36
NG_007878.1:g.2237G>C , LRG_115:g.2237G>C
NG_017040.1:g.10636G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.373-1G>C MANE Select	ENSP00000315774.5:n.373-1G>C
ENST00000313468.9:c.373-1G>C	ENSP00000315774.5:n.373-1G>C
ENST00000524810.5:c.305-1G>C
ENST00000525419.5:c.319-1G>C	ENSP00000433521.1:n.319-1G>C
ENST00000526339.5:c.373-1G>C	ENSP00000436287.1:n.373-1G>C
ENST00000526446.5:c.*428-1G>C	ENSP00000433645.1:n.*428-1G>C
ENST00000526542.1:n.324-1G>C
ENST00000528492.1:c.-66-1G>C	ENSP00000432848.1:n.-66-1G>C
ENST00000531282.1:n.224G>C
NM_002496.3:c.373-1G>C	NP_002487.1:n.373-1G>C
XM_005274013.1:c.373-1G>C	XP_005274070.1:n.373-1G>C
XM_005274014.1:c.373-1G>C	XP_005274071.1:n.373-1G>C
XM_005274015.1:c.253-1G>C	XP_005274072.1:n.253-1G>C
XM_011545053.1:c.373-1G>C	XP_011543355.1:n.373-1G>C
NM_002496.4:c.373-1G>C MANE Select	NP_002487.1:n.373-1G>C