Canonical Allele Identifier: CA10763264
Gene: MFN2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1474868

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11984107C>T , CM000663.2:g.11984107C>T GRCh38
NC_000001.10:g.12044164C>T , CM000663.1:g.12044164C>T GRCh37
NC_000001.9:g.11966751C>T NCBI36
NG_007945.1:g.8927C>T , LRG_255:g.8927C>T

Transcript Alleles

HGVS Amino-acid change
NM_001127660.1:c.-5+3623C>T VV NP_001121132.1:p.=
NM_014874.3:c.-5+1993C>T , LRG_255t1:c.-5+1993C>T NP_055689.1:p.=
XM_005263543.2:c.-5+1517C>T XP_005263600.1:p.=
XM_005263545.2:c.-5+1993C>T XP_005263602.1:p.=
XM_005263547.2:c.-5+1993C>T XP_005263604.1:p.=
XM_005263548.2:c.-5+1517C>T XP_005263605.1:p.=
XM_005263543.3:c.-5+1517C>T XP_005263600.1:p.=
XM_005263545.3:c.-5+1993C>T XP_005263602.1:p.=
XM_005263547.3:c.-5+1993C>T XP_005263604.1:p.=
XM_005263548.3:c.-5+1517C>T XP_005263605.1:p.=
XM_024451299.1:c.-5+1517C>T XP_024307067.1:p.=
ENST00000235329.9:c.-5+1993C>T ENSP00000235329.5:p.=
ENST00000412236.1:c.-5+1517C>T ENSP00000412023.1:p.=
ENST00000444836.5:c.-5+3623C>T ENSP00000416338.1:p.=
ENST00000484391.5:n.115+3623C>T
ENST00000490079.5:n.375+1993C>T
ENST00000497302.1:n.195+1993C>T