Canonical Allele Identifier: CA1022487789

Gene: MX2

Linked Data

• dbSNP Id: rs2089365987
• gnomAD v3: 21-41374150-C-G
• gnomAD v4: 21-41374150-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41374150C>G , CM000683.2:g.41374150C>G	GRCh38
NC_000021.8:g.42746077C>G , CM000683.1:g.42746077C>G	GRCh37
NC_000021.7:g.41667947C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330714.8:c.-71-2686C>G MANE Select	ENSP00000333657.3:n.-71-2686C>G
ENST00000418103.2:c.-71-2686C>G	ENSP00000410188.2:n.-71-2686C>G
ENST00000435611.6:c.-71-2686C>G	ENSP00000389256.2:n.-71-2686C>G
ENST00000680862.1:c.-71-2686C>G	ENSP00000506423.1:n.-71-2686C>G
ENST00000330714.7:c.-71-2686C>G	ENSP00000333657.3:n.-71-2686C>G
ENST00000416447.1:c.-72+23C>G	ENSP00000411179.1:n.-72+23C>G
ENST00000418103.1:c.-71-2686C>G	ENSP00000410188.1:n.-71-2686C>G
ENST00000435611.5:c.-71-2686C>G	ENSP00000389256.1:n.-71-2686C>G
ENST00000436410.5:c.-72+1151C>G	ENSP00000393975.1:n.-72+1151C>G
NM_002463.1:c.-71-2686C>G	NP_002454.1:n.-71-2686C>G
XM_005260983.3:c.-71-2686C>G	XP_005261040.1:n.-71-2686C>G
XM_005260984.1:c.-71-2686C>G	XP_005261041.1:n.-71-2686C>G
XM_011529571.1:c.-72+1151C>G	XP_011527873.1:n.-72+1151C>G
XM_011529572.1:c.-72+23C>G	XP_011527874.1:n.-72+23C>G
XM_011529573.1:c.-71-2686C>G	XP_011527875.1:n.-71-2686C>G
XM_005260983.5:c.-71-2686C>G	XP_005261040.1:n.-71-2686C>G
XM_011529572.2:c.-72+23C>G	XP_011527874.1:n.-72+23C>G
XM_011529573.2:c.-71-2686C>G	XP_011527875.1:n.-71-2686C>G
XM_024452080.1:c.-71-2686C>G	XP_024307848.1:n.-71-2686C>G
NM_002463.2:c.-71-2686C>G MANE Select	NP_002454.1:n.-71-2686C>G