Canonical Allele Identifier: CA2577209091

Gene: NDUFB3

Linked Data

• gnomAD v4: 2-201079029-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201079029T>C , CM000664.2:g.201079029T>C	GRCh38
NC_000002.11:g.201943752T>C , CM000664.1:g.201943752T>C	GRCh37
NC_000002.10:g.201651997T>C	NCBI36
NG_032156.1:g.12291T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450023.6:c.140+7T>C	ENSP00000401834.2:n.140+7T>C
ENST00000682325.1:c.140+7T>C	ENSP00000507925.1:n.140+7T>C
ENST00000684175.1:c.140+7T>C	ENSP00000508132.1:n.140+7T>C
ENST00000684420.1:c.140+7T>C	ENSP00000508208.1:n.140+7T>C
ENST00000237889.9:c.140+7T>C MANE Select	ENSP00000237889.4:n.140+7T>C
ENST00000237889.8:c.140+7T>C	ENSP00000237889.4:n.140+7T>C
ENST00000433898.5:c.140+7T>C	ENSP00000410600.1:n.140+7T>C
ENST00000450023.5:c.140+7T>C	ENSP00000401834.1:n.140+7T>C
ENST00000454214.1:c.140+7T>C	ENSP00000407336.1:n.140+7T>C
NM_001257102.1:c.140+7T>C	NP_001244031.1:n.140+7T>C
NM_002491.2:c.140+7T>C	NP_002482.1:n.140+7T>C
XM_011511230.1:c.140+7T>C	XP_011509532.1:n.140+7T>C
XM_011511230.3:c.140+7T>C	XP_011509532.1:n.140+7T>C
XM_017004186.2:c.140+7T>C	XP_016859675.1:n.140+7T>C
NM_002491.3:c.140+7T>C MANE Select	NP_002482.1:n.140+7T>C
NM_001257102.2:c.140+7T>C	NP_001244031.1:n.140+7T>C