Canonical Allele Identifier: CA2614693264

Gene: NDUFS8

Linked Data

• gnomAD v4: 11-68036629-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036629A>C , CM000673.2:g.68036629A>C	GRCh38
NC_000011.9:g.67804096A>C , CM000673.1:g.67804096A>C	GRCh37
NC_000011.8:g.67560672A>C	NCBI36
NG_007878.1:g.2614A>C , LRG_115:g.2614A>C
NG_017040.1:g.11013A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.*36A>C MANE Select	ENSP00000315774.5:n.*36A>C
ENST00000313468.9:c.*36A>C	ENSP00000315774.5:n.*36A>C
ENST00000524810.5:c.601A>C
ENST00000528492.1:c.*36A>C	ENSP00000432848.1:n.*36A>C
ENST00000531282.1:n.521A>C
NM_002496.3:c.*36A>C	NP_002487.1:n.*36A>C
XM_005274013.1:c.*36A>C	XP_005274070.1:n.*36A>C
XM_005274014.1:c.*36A>C	XP_005274071.1:n.*36A>C
XM_005274015.1:c.*36A>C	XP_005274072.1:n.*36A>C
XM_011545053.1:c.*36A>C	XP_011543355.1:n.*36A>C
NM_002496.4:c.*36A>C MANE Select	NP_002487.1:n.*36A>C