Canonical Allele Identifier: CA749425123

Gene: MX2

Linked Data

• dbSNP Id: rs1456587940
• gnomAD v3: 21-41374163-G-A
• gnomAD v4: 21-41374163-G-A
• MyVariant Identifiers: chr21:g.42746090G>A (hg19) ; chr21:g.41374163G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41374163G>A , CM000683.2:g.41374163G>A	GRCh38
NC_000021.8:g.42746090G>A , CM000683.1:g.42746090G>A	GRCh37
NC_000021.7:g.41667960G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000330714.8:c.-71-2673G>A MANE Select	ENSP00000333657.3:n.-71-2673G>A
ENST00000418103.2:c.-71-2673G>A	ENSP00000410188.2:n.-71-2673G>A
ENST00000435611.6:c.-71-2673G>A	ENSP00000389256.2:n.-71-2673G>A
ENST00000680862.1:c.-71-2673G>A	ENSP00000506423.1:n.-71-2673G>A
ENST00000330714.7:c.-71-2673G>A	ENSP00000333657.3:n.-71-2673G>A
ENST00000416447.1:c.-72+36G>A	ENSP00000411179.1:n.-72+36G>A
ENST00000418103.1:c.-71-2673G>A	ENSP00000410188.1:n.-71-2673G>A
ENST00000435611.5:c.-71-2673G>A	ENSP00000389256.1:n.-71-2673G>A
ENST00000436410.5:c.-72+1164G>A	ENSP00000393975.1:n.-72+1164G>A
NM_002463.1:c.-71-2673G>A	NP_002454.1:n.-71-2673G>A
XM_005260983.3:c.-71-2673G>A	XP_005261040.1:n.-71-2673G>A
XM_005260984.1:c.-71-2673G>A	XP_005261041.1:n.-71-2673G>A
XM_011529571.1:c.-72+1164G>A	XP_011527873.1:n.-72+1164G>A
XM_011529572.1:c.-72+36G>A	XP_011527874.1:n.-72+36G>A
XM_011529573.1:c.-71-2673G>A	XP_011527875.1:n.-71-2673G>A
XM_005260983.5:c.-71-2673G>A	XP_005261040.1:n.-71-2673G>A
XM_011529572.2:c.-72+36G>A	XP_011527874.1:n.-72+36G>A
XM_011529573.2:c.-71-2673G>A	XP_011527875.1:n.-71-2673G>A
XM_024452080.1:c.-71-2673G>A	XP_024307848.1:n.-71-2673G>A
NM_002463.2:c.-71-2673G>A MANE Select	NP_002454.1:n.-71-2673G>A