Canonical Allele Identifier: CA381569106

Gene: NDUFS8

Linked Data

• dbSNP Id: rs1854890244
• gnomAD v4: 11-68036314-T-C
• MyVariant Identifiers: chr11:g.67803781T>C (hg19) ; chr11:g.68036314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.68036314T>C , CM000673.2:g.68036314T>C	GRCh38
NC_000011.9:g.67803781T>C , CM000673.1:g.67803781T>C	GRCh37
NC_000011.8:g.67560357T>C	NCBI36
NG_007878.1:g.2299T>C , LRG_115:g.2299T>C
NG_017040.1:g.10698T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313468.10:c.434T>C MANE Select	ENSP00000315774.5:p.Ile145Thr
ENST00000313468.9:c.434T>C	ENSP00000315774.5:p.Ile145Thr
ENST00000524810.5:c.366T>C
ENST00000525419.5:c.380T>C	ENSP00000433521.1:p.Ile127Thr
ENST00000526339.5:c.434T>C	ENSP00000436287.1:p.Ile145Thr
ENST00000526446.5:c.*489T>C	ENSP00000433645.1:n.*489T>C
ENST00000528492.1:c.-5T>C	ENSP00000432848.1:n.-5T>C
ENST00000531282.1:n.286T>C
NM_002496.3:c.434T>C	NP_002487.1:p.Ile145Thr
XM_005274013.1:c.434T>C	XP_005274070.1:p.Ile145Thr
XM_005274014.1:c.434T>C	XP_005274071.1:p.Ile145Thr
XM_005274015.1:c.314T>C	XP_005274072.1:p.Ile105Thr
XM_011545053.1:c.434T>C	XP_011543355.1:p.Ile145Thr
NM_002496.4:c.434T>C MANE Select	NP_002487.1:p.Ile145Thr