Canonical Allele Identifier: CA475443085

Gene: NDUFS8

Linked Data

• MyVariant Identifiers: chr11:g.67804036C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036569C>T , CM000673.2:g.68036569C>T	GRCh38
NC_000011.9:g.67804036C>T , CM000673.1:g.67804036C>T	GRCh37
NC_000011.8:g.67560612C>T	NCBI36
NG_007878.1:g.2554C>T , LRG_115:g.2554C>T
NG_017040.1:g.10953C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.609C>T MANE Select	ENSP00000315774.5:p.Ile203=
ENST00000313468.9:c.609C>T	ENSP00000315774.5:p.Ile203=
ENST00000524810.5:c.541C>T
ENST00000528492.1:c.171C>T	ENSP00000432848.1:p.Ile57=
ENST00000531282.1:n.461C>T
NM_002496.3:c.609C>T	NP_002487.1:p.Ile203=
XM_005274013.1:c.609C>T	XP_005274070.1:p.Ile203=
XM_005274014.1:c.609C>T	XP_005274071.1:p.Ile203=
XM_005274015.1:c.489C>T	XP_005274072.1:p.Ile163=
XM_011545053.1:c.609C>T	XP_011543355.1:p.Ile203=
NM_002496.4:c.609C>T MANE Select	NP_002487.1:p.Ile203=