Canonical Allele Identifier: CA346074544

Gene: ASXL2

Linked Data

• dbSNP Id: rs1281927825
• gnomAD v4: 2-25742316-G-A
• COSMIC: COSM4492710 ; COSM4492711
• MyVariant Identifiers: chr2:g.25965185G>A (hg19) ; chr2:g.25742316G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742316G>A , CM000664.2:g.25742316G>A	GRCh38
NC_000002.11:g.25965185G>A , CM000664.1:g.25965185G>A	GRCh37
NC_000002.10:g.25818689G>A	NCBI36
NG_052995.1:g.141201C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4018C>T	ENSP00000337250.5:p.His1340Tyr
ENST00000435504.9:c.4021C>T MANE Select	ENSP00000391447.3:p.His1341Tyr
ENST00000336112.8:c.3937C>T	ENSP00000337250.4:p.His1313Tyr
ENST00000404843.5:c.2470C>T	ENSP00000383920.1:p.His824Tyr
ENST00000435504.8:c.4021C>T	ENSP00000391447.3:p.His1341Tyr
NM_018263.4:c.4021C>T	NP_060733.4:p.His1341Tyr
XM_006712039.2:c.3655C>T	XP_006712102.1:p.His1219Tyr
XM_006712040.1:c.3241C>T	XP_006712103.1:p.His1081Tyr
XM_011532950.1:c.4018C>T	XP_011531252.1:p.His1340Tyr
XM_011532951.1:c.3847C>T	XP_011531253.1:p.His1283Tyr
NM_018263.5:c.4021C>T	NP_060733.4:p.His1341Tyr
XM_006712039.3:c.3655C>T	XP_006712102.1:p.His1219Tyr
XM_006712040.2:c.3241C>T	XP_006712103.1:p.His1081Tyr
XM_011532950.3:c.4018C>T	XP_011531252.1:p.His1340Tyr
XM_011532951.2:c.3847C>T	XP_011531253.1:p.His1283Tyr
XM_017004430.1:c.3241C>T	XP_016859919.1:p.His1081Tyr
XM_024452974.1:c.4201C>T	XP_024308742.1:p.His1401Tyr
NM_001369346.1:c.3847C>T	NP_001356275.1:p.His1283Tyr
NM_001369347.1:c.3241C>T	NP_001356276.1:p.His1081Tyr
NM_018263.6:c.4021C>T MANE Select	NP_060733.4:p.His1341Tyr