Canonical Allele Identifier: CA2675613317

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.140647633C>A , CM000667.2:g.140647633C>A GRCh38
NC_000005.9:g.140027218C>A , CM000667.1:g.140027218C>A GRCh37
NC_000005.8:g.140007402C>A NCBI36
NG_021417.1:g.5153G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252102.8:c.-50G>T (NDUFA2) ENSP00000252102.4:n.-50G>T
ENST00000502960.1:n.139G>T (NDUFA2)
ENST00000512088.1:c.-50G>T (NDUFA2) ENSP00000427220.1:n.-50G>T
ENST00000513256.5:c.4+324C>A (IK) ENSP00000425564.1:n.4+324C>A
NM_001185012.1:c.-50G>T (NDUFA2) NP_001171941.1:n.-50G>T
NM_002488.4:c.-50G>T (NDUFA2) NP_002479.1:n.-50G>T
NR_033697.1:n.153G>T (NDUFA2)