Canonical Allele Identifier: CA475442828

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67803979C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036512C>T , CM000673.2:g.68036512C>T	GRCh38
NC_000011.9:g.67803979C>T , CM000673.1:g.67803979C>T	GRCh37
NC_000011.8:g.67560555C>T	NCBI36
NG_007878.1:g.2497C>T , LRG_115:g.2497C>T
NG_017040.1:g.10896C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313468.10:c.552C>T MANE Select	ENSP00000315774.5:p.Asn184=
ENST00000313468.9:c.552C>T	ENSP00000315774.5:p.Asn184=
ENST00000524810.5:c.484C>T
ENST00000526339.5:c.552C>T	ENSP00000436287.1:p.Asn184=
ENST00000526446.5:c.*607C>T	ENSP00000433645.1:n.*607C>T
ENST00000528492.1:c.114C>T	ENSP00000432848.1:p.Asn38=
ENST00000531282.1:n.404C>T
NM_002496.3:c.552C>T	NP_002487.1:p.Asn184=
XM_005274013.1:c.552C>T	XP_005274070.1:p.Asn184=
XM_005274014.1:c.552C>T	XP_005274071.1:p.Asn184=
XM_005274015.1:c.432C>T	XP_005274072.1:p.Asn144=
XM_011545053.1:c.552C>T	XP_011543355.1:p.Asn184=
NM_002496.4:c.552C>T MANE Select	NP_002487.1:p.Asn184=