Canonical Allele Identifier: CA502964528
Gene: AFG3L2 HGNC NCBI
TUBB6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.12337493G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.12337494G>C , CM000680.2:g.12337494G>C GRCh38
NC_000018.9:g.12337493G>C , CM000680.1:g.12337493G>C GRCh37
NC_000018.8:g.12327493G>C NCBI36
NG_023361.1:g.44783C>G , LRG_666:g.44783C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000687337.1:c.*1618C>G (AFG3L2) ENSP00000508998.1:n.*1618C>G
ENST00000687477.1:n.558C>G (AFG3L2)
ENST00000688199.1:c.1884C>G (AFG3L2) ENSP00000510237.1:p.Ser628=
ENST00000691179.1:c.1947C>G (AFG3L2) ENSP00000509010.1:p.Ser649=
ENST00000691970.1:c.*1399C>G (AFG3L2) ENSP00000508440.1:n.*1399C>G
ENST00000692497.1:c.*452C>G (AFG3L2) ENSP00000509870.1:n.*452C>G
ENST00000692988.1:n.1840C>G (AFG3L2)
ENST00000269143.8:c.2022C>G (AFG3L2) MANE Select ENSP00000269143.2:p.Ser674=
ENST00000269143.7:c.2022C>G (AFG3L2) ENSP00000269143.2:p.Ser674=
ENST00000586691.1:c.88-6555G>C (TUBB6)
NM_006796.2:c.2022C>G , LRG_666t1:c.2022C>G (AFG3L2) NP_006787.2:p.Ser674=
XM_011525601.1:c.1821C>G (AFG3L2) XP_011523903.1:p.Ser607=
XM_011525601.3:c.1821C>G (AFG3L2) XP_011523903.1:p.Ser607=
XR_002958227.1:n.451+592G>C
NM_006796.3:c.2022C>G (AFG3L2) MANE Select NP_006787.2:p.Ser674=