Canonical Allele Identifier: CA296690266

Gene: AFG3L2 TUBB6

Linked Data

• dbSNP Id: rs915219018
• MyVariant Identifiers: chr18:g.12337402T>C (hg19) ; chr18:g.12337403T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337403T>C , CM000680.2:g.12337403T>C	GRCh38
NC_000018.9:g.12337402T>C , CM000680.1:g.12337402T>C	GRCh37
NC_000018.8:g.12327402T>C	NCBI36
NG_023361.1:g.44874A>G , LRG_666:g.44874A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1709A>G (AFG3L2)	ENSP00000508998.1:n.*1709A>G
ENST00000687477.1:n.649A>G (AFG3L2)
ENST00000688199.1:c.1975A>G (AFG3L2)	ENSP00000510237.1:p.Ile659Val
ENST00000691179.1:c.2038A>G (AFG3L2)	ENSP00000509010.1:p.Ile680Val
ENST00000691970.1:c.*1490A>G (AFG3L2)	ENSP00000508440.1:n.*1490A>G
ENST00000692497.1:c.*543A>G (AFG3L2)	ENSP00000509870.1:n.*543A>G
ENST00000692988.1:n.1931A>G (AFG3L2)
ENST00000269143.8:c.2113A>G (AFG3L2) MANE Select	ENSP00000269143.2:p.Ile705Val
ENST00000269143.7:c.2113A>G (AFG3L2)	ENSP00000269143.2:p.Ile705Val
ENST00000586691.1:c.88-6646T>C (TUBB6)
NM_006796.2:c.2113A>G , LRG_666t1:c.2113A>G (AFG3L2)	NP_006787.2:p.Ile705Val
XM_011525601.1:c.1912A>G (AFG3L2)	XP_011523903.1:p.Ile638Val
XM_011525601.3:c.1912A>G (AFG3L2)	XP_011523903.1:p.Ile638Val
XR_002958227.1:n.451+501T>C
NM_006796.3:c.2113A>G (AFG3L2) MANE Select	NP_006787.2:p.Ile705Val