Canonical Allele Identifier: CA1153896775
Gene: MFN2 HGNC NCBI

Linked Data

dbSNP Id: rs1432585482
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.11980191G>A , CM000663.2:g.11980191G>A GRCh38
NC_000001.10:g.12040248G>A , CM000663.1:g.12040248G>A GRCh37
NC_000001.9:g.11962835G>A NCBI36
NG_007945.1:g.5011G>A , LRG_255:g.5011G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000674817.1:c.-298G>A ENSP00000502151.1:n.-298G>A
ENST00000675053.1:c.-346G>A ENSP00000501646.1:n.-346G>A
ENST00000444836.5:c.-298G>A ENSP00000416338.1:n.-298G>A
NM_001127660.1:c.-298G>A NP_001121132.1:n.-298G>A
NM_014874.3:c.-443G>A , LRG_255t1:c.-443G>A NP_055689.1:n.-443G>A
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