Canonical Allele Identifier: CA346076095

Gene: ASXL2

Linked Data

• ClinVar Variation Id: 3062134
• ClinVar RCV Id: RCV003985244
• dbSNP Id: rs1236056808
• gnomAD v2: 2-25965422-C-A
• gnomAD v3: 2-25742553-C-A
• gnomAD v4: 2-25742553-C-A
• MyVariant Identifiers: chr2:g.25965422C>A (hg19) ; chr2:g.25742553C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742553C>A , CM000664.2:g.25742553C>A	GRCh38
NC_000002.11:g.25965422C>A , CM000664.1:g.25965422C>A	GRCh37
NC_000002.10:g.25818926C>A	NCBI36
NG_052995.1:g.140964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3781G>T	ENSP00000337250.5:p.Ala1261Ser
ENST00000435504.9:c.3784G>T MANE Select	ENSP00000391447.3:p.Ala1262Ser
ENST00000336112.8:c.3700G>T	ENSP00000337250.4:p.Ala1234Ser
ENST00000404843.5:c.2233G>T	ENSP00000383920.1:p.Ala745Ser
ENST00000435504.8:c.3784G>T	ENSP00000391447.3:p.Ala1262Ser
NM_018263.4:c.3784G>T	NP_060733.4:p.Ala1262Ser
XM_006712039.2:c.3418G>T	XP_006712102.1:p.Ala1140Ser
XM_006712040.1:c.3004G>T	XP_006712103.1:p.Ala1002Ser
XM_011532950.1:c.3781G>T	XP_011531252.1:p.Ala1261Ser
XM_011532951.1:c.3610G>T	XP_011531253.1:p.Ala1204Ser
NM_018263.5:c.3784G>T	NP_060733.4:p.Ala1262Ser
XM_006712039.3:c.3418G>T	XP_006712102.1:p.Ala1140Ser
XM_006712040.2:c.3004G>T	XP_006712103.1:p.Ala1002Ser
XM_011532950.3:c.3781G>T	XP_011531252.1:p.Ala1261Ser
XM_011532951.2:c.3610G>T	XP_011531253.1:p.Ala1204Ser
XM_017004430.1:c.3004G>T	XP_016859919.1:p.Ala1002Ser
XM_024452974.1:c.3964G>T	XP_024308742.1:p.Ala1322Ser
NM_001369346.1:c.3610G>T	NP_001356275.1:p.Ala1204Ser
NM_001369347.1:c.3004G>T	NP_001356276.1:p.Ala1002Ser
NM_018263.6:c.3784G>T MANE Select	NP_060733.4:p.Ala1262Ser