Canonical Allele Identifier: CA503244777
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.12337415T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337416T>C , CM000680.2:g.12337416T>C GRCh38
NC_000018.9:g.12337415T>C , CM000680.1:g.12337415T>C GRCh37
NC_000018.8:g.12327415T>C NCBI36
NG_023361.1:g.44861A>G , LRG_666:g.44861A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000687337.1:c.*1696A>G (AFG3L2) ENSP00000508998.1:n.*1696A>G
ENST00000687477.1:n.636A>G (AFG3L2)
ENST00000688199.1:c.1962A>G (AFG3L2) ENSP00000510237.1:p.Glu654=
ENST00000691179.1:c.2025A>G (AFG3L2) ENSP00000509010.1:p.Glu675=
ENST00000691970.1:c.*1477A>G (AFG3L2) ENSP00000508440.1:n.*1477A>G
ENST00000692497.1:c.*530A>G (AFG3L2) ENSP00000509870.1:n.*530A>G
ENST00000692988.1:n.1918A>G (AFG3L2)
ENST00000269143.8:c.2100A>G (AFG3L2) MANE Select ENSP00000269143.2:p.Glu700=
ENST00000269143.7:c.2100A>G (AFG3L2) ENSP00000269143.2:p.Glu700=
ENST00000586691.1:c.88-6633T>C (TUBB6)
NM_006796.2:c.2100A>G , LRG_666t1:c.2100A>G (AFG3L2) NP_006787.2:p.Glu700=
XM_011525601.1:c.1899A>G (AFG3L2) XP_011523903.1:p.Glu633=
XM_011525601.3:c.1899A>G (AFG3L2) XP_011523903.1:p.Glu633=
XR_002958227.1:n.451+514T>C
NM_006796.3:c.2100A>G (AFG3L2) MANE Select NP_006787.2:p.Glu700=