Canonical Allele Identifier: CA1211968213
Gene: NCF2 HGNC NCBI
SMG7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590705T= , CM000663.2:g.183590705T= GRCh38
NC_000001.10:g.183559840T= , CM000663.1:g.183559840T= GRCh37
NC_000001.9:g.181826463T= NCBI36
NG_007267.1:g.4877A= , LRG_88:g.4877A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-31+135A= (NCF2) ENSP00000513258.1:n.-31+135A=
ENST00000697353.1:n.1A= (NCF2)
ENST00000367536.5:c.-31+135A= (NCF2) ENSP00000356506.1:n.-31+135A=
ENST00000495321.1:n.234-7064T= (SMG7)
NM_001127651.2:c.-31+135A= (NCF2) NP_001121123.1:n.-31+135A=
XM_011509580.1:c.-113A= (NCF2) XP_011507882.1:n.-113A=
NM_001127651.3:c.-31+135A= (NCF2) NP_001121123.1:n.-31+135A=
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