Canonical Allele Identifier: CA1211968187

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590637G= , CM000663.2:g.183590637G= GRCh38
NC_000001.10:g.183559772G= , CM000663.1:g.183559772G= GRCh37
NC_000001.9:g.181826395G= NCBI36
NG_007267.1:g.4945C= , LRG_88:g.4945C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-31+203C= (NCF2) ENSP00000513258.1:n.-31+203C=
ENST00000697353.1:n.69C= (NCF2)
ENST00000367536.5:c.-31+203C= (NCF2) ENSP00000356506.1:n.-31+203C=
ENST00000495321.1:n.234-7132G= (SMG7)
NM_001127651.2:c.-31+203C= (NCF2) NP_001121123.1:n.-31+203C=
XM_011509580.1:c.-45C= (NCF2) XP_011507882.1:n.-45C=
NM_001127651.3:c.-31+203C= (NCF2) NP_001121123.1:n.-31+203C=