Canonical Allele Identifier: CA749428951

Gene: MX2

Linked Data

• dbSNP Id: rs1375603336
• gnomAD v3: 21-41380422-C-A
• gnomAD v4: 21-41380422-C-A
• MyVariant Identifiers: chr21:g.42752349C>A (hg19) ; chr21:g.41380422C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.41380422C>A , CM000683.2:g.41380422C>A	GRCh38
NC_000021.8:g.42752349C>A , CM000683.1:g.42752349C>A	GRCh37
NC_000021.7:g.41674219C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000330714.8:c.577+271C>A MANE Select	ENSP00000333657.3:n.577+271C>A
ENST00000418103.2:c.443-1988C>A	ENSP00000410188.2:n.443-1988C>A
ENST00000435611.6:c.577+271C>A	ENSP00000389256.2:n.577+271C>A
ENST00000493753.2:n.634+271C>A
ENST00000680862.1:c.577+271C>A	ENSP00000506423.1:n.577+271C>A
ENST00000330714.7:c.577+271C>A	ENSP00000333657.3:n.577+271C>A
NM_002463.1:c.577+271C>A	NP_002454.1:n.577+271C>A
XM_005260983.3:c.577+271C>A	XP_005261040.1:n.577+271C>A
XM_005260984.1:c.577+271C>A	XP_005261041.1:n.577+271C>A
XM_011529571.1:c.577+271C>A	XP_011527873.1:n.577+271C>A
XM_011529572.1:c.577+271C>A	XP_011527874.1:n.577+271C>A
XM_011529573.1:c.443-1988C>A	XP_011527875.1:n.443-1988C>A
XM_005260983.5:c.577+271C>A	XP_005261040.1:n.577+271C>A
XM_011529572.2:c.577+271C>A	XP_011527874.1:n.577+271C>A
XM_011529573.2:c.443-1988C>A	XP_011527875.1:n.443-1988C>A
XM_024452080.1:c.577+271C>A	XP_024307848.1:n.577+271C>A
NM_002463.2:c.577+271C>A MANE Select	NP_002454.1:n.577+271C>A