Canonical Allele Identifier: CA2649486343
Gene: NCF2 HGNC NCBI
SMG7 HGNC NCBI

Linked Data

gnomAD v4: 1-183590691-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.183590691T>A , CM000663.2:g.183590691T>A GRCh38
NC_000001.10:g.183559826T>A , CM000663.1:g.183559826T>A GRCh37
NC_000001.9:g.181826449T>A NCBI36
NG_007267.1:g.4891A>T , LRG_88:g.4891A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697330.1:c.-31+149A>T (NCF2) ENSP00000513258.1:n.-31+149A>T
ENST00000697353.1:n.15A>T (NCF2)
ENST00000367536.5:c.-31+149A>T (NCF2) ENSP00000356506.1:n.-31+149A>T
ENST00000495321.1:n.234-7078T>A (SMG7)
NM_001127651.2:c.-31+149A>T (NCF2) NP_001121123.1:n.-31+149A>T
XM_011509580.1:c.-99A>T (NCF2) XP_011507882.1:n.-99A>T
NM_001127651.3:c.-31+149A>T (NCF2) NP_001121123.1:n.-31+149A>T
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