Canonical Allele Identifier: CA4871473

Gene: NDUFB9

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.124543094T>C , CM000670.2:g.124543094T>C	GRCh38
NC_000008.10:g.125555335T>C , CM000670.1:g.125555335T>C	GRCh37
NC_000008.9:g.125624516T>C	NCBI36
NG_042266.1:g.8993T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_005005.3:c.109T>C MANE Select	NP_004996.1:p.Tyr37His
ENST00000276689.8:c.109T>C MANE Select	ENSP00000276689.3:p.Tyr37His
NM_001278645.1:c.-32-28T>C	NP_001265574.1:n.-32-28T>C
NM_001278645.2:c.-32-28T>C	NP_001265574.1:n.-32-28T>C
NM_001278646.1:c.-21T>C	NP_001265575.1:n.-21T>C
NM_001278646.2:c.-21T>C	NP_001265575.1:n.-21T>C
NM_001311168.1:c.102-26T>C	NP_001298097.1:n.102-26T>C
NM_001311168.2:c.102-26T>C	NP_001298097.1:n.102-26T>C
NM_005005.2:c.109T>C	NP_004996.1:p.Tyr37His
ENST00000276689.7:c.109T>C	ENSP00000276689.3:p.Tyr37His
ENST00000517367.1:c.102-26T>C	ENSP00000430322.1:n.102-26T>C
ENST00000518008.5:c.109T>C	ENSP00000428282.1:p.Tyr37His
ENST00000518657.5:n.155T>C
ENST00000518657.6:n.1189T>C
ENST00000522532.5:c.109T>C	ENSP00000431115.1:p.Tyr37His
ENST00000522532.6:c.109T>C	ENSP00000431115.1:p.Tyr37His
ENST00000524241.2:n.134T>C
ENST00000606244.2:c.109T>C	ENSP00000497750.1:p.Tyr37His
ENST00000676713.1:c.107T>C	ENSP00000504795.1:p.Ile36Thr
ENST00000677021.1:c.109T>C	ENSP00000504235.1:p.Tyr37His
ENST00000677782.1:n.128T>C
ENST00000677822.1:c.109T>C	ENSP00000504813.1:p.Tyr37His
ENST00000677950.1:c.107T>C	ENSP00000504071.1:p.Ile36Thr