Canonical Allele Identifier: CA1082226389

Linked Data

dbSNP Id: rs1246663582

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647619C>G , CM000667.2:g.140647619C>G GRCh38
NC_000005.9:g.140027204C>G , CM000667.1:g.140027204C>G GRCh37
NC_000005.8:g.140007388C>G NCBI36
NG_021417.1:g.5167G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252102.9:c.-36G>C (NDUFA2) MANE Select ENSP00000252102.5:n.-36G>C
ENST00000252102.8:c.-36G>C (NDUFA2) ENSP00000252102.4:n.-36G>C
ENST00000502960.1:n.153G>C (NDUFA2)
ENST00000512088.1:c.-36G>C (NDUFA2) ENSP00000427220.1:n.-36G>C
ENST00000513256.5:c.4+310C>G (IK) ENSP00000425564.1:n.4+310C>G
NM_001185012.1:c.-36G>C (NDUFA2) NP_001171941.1:n.-36G>C
NM_002488.4:c.-36G>C (NDUFA2) NP_002479.1:n.-36G>C
NR_033697.1:n.167G>C (NDUFA2)
NM_002488.5:c.-36G>C (NDUFA2) MANE Select NP_002479.1:n.-36G>C
NM_001185012.2:c.-36G>C (NDUFA2) NP_001171941.1:n.-36G>C
NR_033697.2:n.12G>C (NDUFA2)