Canonical Allele Identifier: CA1153896834

Gene: MFN2

Linked Data

• dbSNP Id: rs1470702496
• gnomAD v4: 1-11980270-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.11980270C>T , CM000663.2:g.11980270C>T	GRCh38
NC_000001.10:g.12040327C>T , CM000663.1:g.12040327C>T	GRCh37
NC_000001.9:g.11962914C>T	NCBI36
NG_007945.1:g.5090C>T , LRG_255:g.5090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000412236.2:c.-428C>T	ENSP00000412023.1:n.-428C>T
ENST00000674548.1:c.-309C>T	ENSP00000502185.1:n.-309C>T
ENST00000674706.1:n.12C>T
ENST00000674817.1:c.-219C>T	ENSP00000502151.1:n.-219C>T
ENST00000675053.1:c.-267C>T	ENSP00000501646.1:n.-267C>T
ENST00000675194.1:n.62C>T
ENST00000675298.1:c.-364C>T	ENSP00000501839.1:n.-364C>T
ENST00000675530.1:c.-360C>T	ENSP00000501972.1:n.-360C>T
ENST00000675817.1:c.-364C>T	ENSP00000502422.1:n.-364C>T
ENST00000675872.1:n.33C>T
ENST00000675959.1:n.34C>T
ENST00000676369.1:c.-432C>T	ENSP00000502005.1:n.-432C>T
ENST00000676426.1:c.-364C>T	ENSP00000502359.1:n.-364C>T
ENST00000444836.5:c.-219C>T	ENSP00000416338.1:n.-219C>T
NM_001127660.1:c.-219C>T	NP_001121132.1:n.-219C>T
NM_014874.3:c.-364C>T , LRG_255t1:c.-364C>T	NP_055689.1:n.-364C>T
XM_005263543.2:c.-432C>T	XP_005263600.1:n.-432C>T
XM_005263548.2:c.-428C>T	XP_005263605.1:n.-428C>T
XM_005263543.3:c.-432C>T	XP_005263600.1:n.-432C>T
XM_005263548.3:c.-428C>T	XP_005263605.1:n.-428C>T