Canonical Allele Identifier: CA346075535

Gene: ASXL2

Linked Data

• ClinVar Variation Id: 2688621
• ClinVar RCV Id: RCV003492918
• dbSNP Id: rs2149135782
• MyVariant Identifiers: chr2:g.25965337C>T (hg19) ; chr2:g.25742468C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742468C>T , CM000664.2:g.25742468C>T	GRCh38
NC_000002.11:g.25965337C>T , CM000664.1:g.25965337C>T	GRCh37
NC_000002.10:g.25818841C>T	NCBI36
NG_052995.1:g.141049G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3866G>A	ENSP00000337250.5:p.Ser1289Asn
ENST00000435504.9:c.3869G>A MANE Select	ENSP00000391447.3:p.Ser1290Asn
ENST00000336112.8:c.3785G>A	ENSP00000337250.4:p.Ser1262Asn
ENST00000404843.5:c.2318G>A	ENSP00000383920.1:p.Ser773Asn
ENST00000435504.8:c.3869G>A	ENSP00000391447.3:p.Ser1290Asn
NM_018263.4:c.3869G>A	NP_060733.4:p.Ser1290Asn
XM_006712039.2:c.3503G>A	XP_006712102.1:p.Ser1168Asn
XM_006712040.1:c.3089G>A	XP_006712103.1:p.Ser1030Asn
XM_011532950.1:c.3866G>A	XP_011531252.1:p.Ser1289Asn
XM_011532951.1:c.3695G>A	XP_011531253.1:p.Ser1232Asn
NM_018263.5:c.3869G>A	NP_060733.4:p.Ser1290Asn
XM_006712039.3:c.3503G>A	XP_006712102.1:p.Ser1168Asn
XM_006712040.2:c.3089G>A	XP_006712103.1:p.Ser1030Asn
XM_011532950.3:c.3866G>A	XP_011531252.1:p.Ser1289Asn
XM_011532951.2:c.3695G>A	XP_011531253.1:p.Ser1232Asn
XM_017004430.1:c.3089G>A	XP_016859919.1:p.Ser1030Asn
XM_024452974.1:c.4049G>A	XP_024308742.1:p.Ser1350Asn
NM_001369346.1:c.3695G>A	NP_001356275.1:p.Ser1232Asn
NM_001369347.1:c.3089G>A	NP_001356276.1:p.Ser1030Asn
NM_018263.6:c.3869G>A MANE Select	NP_060733.4:p.Ser1290Asn