Canonical Allele Identifier: CA8896324

Gene: AFG3L2 TUBB6

Linked Data

• dbSNP Id: rs771589955
• ExAC: 18:12337507 C / T
• gnomAD v2: 18-12337507-C-T
• gnomAD v4: 18-12337508-C-T
• MyVariant Identifiers: chr18:g.12337507C>T (hg19) ; chr18:g.12337508C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337508C>T , CM000680.2:g.12337508C>T	GRCh38
NC_000018.9:g.12337507C>T , CM000680.1:g.12337507C>T	GRCh37
NC_000018.8:g.12327507C>T	NCBI36
NG_023361.1:g.44769G>A , LRG_666:g.44769G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1604G>A (AFG3L2)	ENSP00000508998.1:n.*1604G>A
ENST00000687477.1:n.544G>A (AFG3L2)
ENST00000688199.1:c.1870G>A (AFG3L2)	ENSP00000510237.1:p.Val624Ile
ENST00000691179.1:c.1933G>A (AFG3L2)	ENSP00000509010.1:p.Val645Ile
ENST00000691970.1:c.*1385G>A (AFG3L2)	ENSP00000508440.1:n.*1385G>A
ENST00000692497.1:c.*438G>A (AFG3L2)	ENSP00000509870.1:n.*438G>A
ENST00000692988.1:n.1826G>A (AFG3L2)
ENST00000269143.8:c.2008G>A (AFG3L2) MANE Select	ENSP00000269143.2:p.Val670Ile
ENST00000269143.7:c.2008G>A (AFG3L2)	ENSP00000269143.2:p.Val670Ile
ENST00000586691.1:c.88-6541C>T (TUBB6)
NM_006796.2:c.2008G>A , LRG_666t1:c.2008G>A (AFG3L2)	NP_006787.2:p.Val670Ile
XM_011525601.1:c.1807G>A (AFG3L2)	XP_011523903.1:p.Val603Ile
XM_011525601.3:c.1807G>A (AFG3L2)	XP_011523903.1:p.Val603Ile
XR_002958227.1:n.451+606C>T
NM_006796.3:c.2008G>A (AFG3L2) MANE Select	NP_006787.2:p.Val670Ile