Canonical Allele Identifier: CA1980452613

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1812347981
• gnomAD v4: 11-68036625-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036625A>G , CM000673.2:g.68036625A>G	GRCh38
NC_000011.9:g.67804092A>G , CM000673.1:g.67804092A>G	GRCh37
NC_000011.8:g.67560668A>G	NCBI36
NG_007878.1:g.2610A>G , LRG_115:g.2610A>G
NG_017040.1:g.11009A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.*32A>G MANE Select	ENSP00000315774.5:n.*32A>G
ENST00000313468.9:c.*32A>G	ENSP00000315774.5:n.*32A>G
ENST00000524810.5:c.597A>G
ENST00000528492.1:c.*32A>G	ENSP00000432848.1:n.*32A>G
ENST00000531282.1:n.517A>G
NM_002496.3:c.*32A>G	NP_002487.1:n.*32A>G
XM_005274013.1:c.*32A>G	XP_005274070.1:n.*32A>G
XM_005274014.1:c.*32A>G	XP_005274071.1:n.*32A>G
XM_005274015.1:c.*32A>G	XP_005274072.1:n.*32A>G
XM_011545053.1:c.*32A>G	XP_011543355.1:n.*32A>G
NM_002496.4:c.*32A>G MANE Select	NP_002487.1:n.*32A>G