Canonical Allele Identifier: CA776244661

Gene: AFG3L2

Linked Data

• dbSNP Id: rs1421912231
• MyVariant Identifiers: chr18:g.12351009A>G (hg19) ; chr18:g.12351010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351010A>G , CM000680.2:g.12351010A>G	GRCh38
NC_000018.9:g.12351009A>G , CM000680.1:g.12351009A>G	GRCh37
NC_000018.8:g.12341009A>G	NCBI36
NG_023361.1:g.31267T>C , LRG_666:g.31267T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1148+75T>C	ENSP00000508998.1:n.*1148+75T>C
ENST00000688199.1:c.1414+75T>C	ENSP00000510237.1:n.1414+75T>C
ENST00000691179.1:c.1477+75T>C	ENSP00000509010.1:n.1477+75T>C
ENST00000691970.1:c.*929+75T>C	ENSP00000508440.1:n.*929+75T>C
ENST00000692497.1:c.1552+75T>C	ENSP00000509870.1:n.1552+75T>C
ENST00000692988.1:n.1370+75T>C
ENST00000269143.8:c.1552+75T>C MANE Select	ENSP00000269143.2:n.1552+75T>C
ENST00000269143.7:c.1552+75T>C	ENSP00000269143.2:n.1552+75T>C
NM_006796.2:c.1552+75T>C , LRG_666t1:c.1552+75T>C	NP_006787.2:n.1552+75T>C
XM_011525601.1:c.1552+75T>C	XP_011523903.1:n.1552+75T>C
XM_011525601.3:c.1552+75T>C	XP_011523903.1:n.1552+75T>C
NM_006796.3:c.1552+75T>C MANE Select	NP_006787.2:n.1552+75T>C