Canonical Allele Identifier: CA361216785

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647535G>C , CM000667.2:g.140647535G>C GRCh38
NC_000005.9:g.140027120G>C , CM000667.1:g.140027120G>C GRCh37
NC_000005.8:g.140007304G>C NCBI36
NG_021417.1:g.5251C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.49C>G (NDUFA2) MANE Select ENSP00000252102.5:p.Arg17Gly
ENST00000252102.8:c.49C>G (NDUFA2) ENSP00000252102.4:p.Arg17Gly
ENST00000502960.1:n.237C>G (NDUFA2)
ENST00000512088.1:c.49C>G (NDUFA2) ENSP00000427220.1:p.Arg17Gly
ENST00000513256.5:c.4+226G>C (IK) ENSP00000425564.1:n.4+226G>C
NM_001185012.1:c.49C>G (NDUFA2) NP_001171941.1:p.Arg17Gly
NM_002488.4:c.49C>G (NDUFA2) NP_002479.1:p.Arg17Gly
NR_033697.1:n.251C>G (NDUFA2)
NM_002488.5:c.49C>G (NDUFA2) MANE Select NP_002479.1:p.Arg17Gly
NM_001185012.2:c.49C>G (NDUFA2) NP_001171941.1:p.Arg17Gly
NR_033697.2:n.96C>G (NDUFA2)