Canonical Allele Identifier: CA776237839

Gene: AFG3L2 TUBB6

Linked Data

• dbSNP Id: rs1331641417
• gnomAD v3: 18-12337262-C-G
• gnomAD v4: 18-12337262-C-G
• MyVariant Identifiers: chr18:g.12337261C>G (hg19) ; chr18:g.12337262C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337262C>G , CM000680.2:g.12337262C>G	GRCh38
NC_000018.9:g.12337261C>G , CM000680.1:g.12337261C>G	GRCh37
NC_000018.8:g.12327261C>G	NCBI36
NG_023361.1:g.45015G>C , LRG_666:g.45015G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1771+79G>C (AFG3L2)	ENSP00000508998.1:n.*1771+79G>C
ENST00000687477.1:n.711+79G>C (AFG3L2)
ENST00000688199.1:c.2037+79G>C (AFG3L2)	ENSP00000510237.1:n.2037+79G>C
ENST00000691179.1:c.2100+79G>C (AFG3L2)	ENSP00000509010.1:n.2100+79G>C
ENST00000691970.1:c.*1552+79G>C (AFG3L2)	ENSP00000508440.1:n.*1552+79G>C
ENST00000692497.1:c.*605+79G>C (AFG3L2)	ENSP00000509870.1:n.*605+79G>C
ENST00000692988.1:n.1993+79G>C (AFG3L2)
ENST00000269143.8:c.2175+79G>C (AFG3L2) MANE Select	ENSP00000269143.2:n.2175+79G>C
ENST00000269143.7:c.2175+79G>C (AFG3L2)	ENSP00000269143.2:n.2175+79G>C
ENST00000586691.1:c.88-6787C>G (TUBB6)
NM_006796.2:c.2175+79G>C , LRG_666t1:c.2175+79G>C (AFG3L2)	NP_006787.2:n.2175+79G>C
XM_011525601.1:c.1974+79G>C (AFG3L2)	XP_011523903.1:n.1974+79G>C
XM_011525601.3:c.1974+79G>C (AFG3L2)	XP_011523903.1:n.1974+79G>C
XR_002958227.1:n.451+360C>G
NM_006796.3:c.2175+79G>C (AFG3L2) MANE Select	NP_006787.2:n.2175+79G>C