Canonical Allele Identifier: CA1140353455

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590706G= , CM000663.2:g.183590706G= GRCh38
NC_000001.10:g.183559841G= , CM000663.1:g.183559841G= GRCh37
NC_000001.9:g.181826464G= NCBI36
NG_007267.1:g.4876C= , LRG_88:g.4876C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-31+134C= (NCF2) ENSP00000513258.1:n.-31+134C=
ENST00000367536.5:c.-31+134C= (NCF2) ENSP00000356506.1:n.-31+134C=
ENST00000495321.1:n.234-7063G= (SMG7)
NM_001127651.2:c.-31+134C= (NCF2) NP_001121123.1:n.-31+134C=
NM_001127651.3:c.-31+134C= (NCF2) NP_001121123.1:n.-31+134C=