Canonical Allele Identifier: CA1211968201
Gene: NCF2 HGNC NCBI
SMG7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590665C= , CM000663.2:g.183590665C= GRCh38
NC_000001.10:g.183559800C= , CM000663.1:g.183559800C= GRCh37
NC_000001.9:g.181826423C= NCBI36
NG_007267.1:g.4917G= , LRG_88:g.4917G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-31+175G= (NCF2) ENSP00000513258.1:n.-31+175G=
ENST00000697353.1:n.41G= (NCF2)
ENST00000367536.5:c.-31+175G= (NCF2) ENSP00000356506.1:n.-31+175G=
ENST00000495321.1:n.234-7104C= (SMG7)
NM_001127651.2:c.-31+175G= (NCF2) NP_001121123.1:n.-31+175G=
XM_011509580.1:c.-73G= (NCF2) XP_011507882.1:n.-73G=
NM_001127651.3:c.-31+175G= (NCF2) NP_001121123.1:n.-31+175G=
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