Canonical Allele Identifier: CA502964891

Gene: AFG3L2

Linked Data

• MyVariant Identifiers: chr18:g.12351097A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351098A>C , CM000680.2:g.12351098A>C	GRCh38
NC_000018.9:g.12351097A>C , CM000680.1:g.12351097A>C	GRCh37
NC_000018.8:g.12341097A>C	NCBI36
NG_023361.1:g.31179T>G , LRG_666:g.31179T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1135T>G	ENSP00000508998.1:n.*1135T>G
ENST00000688199.1:c.1401T>G	ENSP00000510237.1:p.Thr467=
ENST00000691179.1:c.1464T>G	ENSP00000509010.1:p.Thr488=
ENST00000691970.1:c.*916T>G	ENSP00000508440.1:n.*916T>G
ENST00000692497.1:c.1539T>G	ENSP00000509870.1:p.Thr513=
ENST00000692988.1:n.1357T>G
ENST00000269143.8:c.1539T>G MANE Select	ENSP00000269143.2:p.Thr513=
ENST00000269143.7:c.1539T>G	ENSP00000269143.2:p.Thr513=
NM_006796.2:c.1539T>G , LRG_666t1:c.1539T>G	NP_006787.2:p.Thr513=
XM_011525601.1:c.1539T>G	XP_011523903.1:p.Thr513=
XM_011525601.3:c.1539T>G	XP_011523903.1:p.Thr513=
NM_006796.3:c.1539T>G MANE Select	NP_006787.2:p.Thr513=