Canonical Allele Identifier: CA346075315

Gene: ASXL2

Linked Data

• gnomAD v4: 2-25742430-G-T
• MyVariant Identifiers: chr2:g.25965299G>T (hg19) ; chr2:g.25742430G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742430G>T , CM000664.2:g.25742430G>T	GRCh38
NC_000002.11:g.25965299G>T , CM000664.1:g.25965299G>T	GRCh37
NC_000002.10:g.25818803G>T	NCBI36
NG_052995.1:g.141087C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3904C>A	ENSP00000337250.5:p.His1302Asn
ENST00000435504.9:c.3907C>A MANE Select	ENSP00000391447.3:p.His1303Asn
ENST00000336112.8:c.3823C>A	ENSP00000337250.4:p.His1275Asn
ENST00000404843.5:c.2356C>A	ENSP00000383920.1:p.His786Asn
ENST00000435504.8:c.3907C>A	ENSP00000391447.3:p.His1303Asn
NM_018263.4:c.3907C>A	NP_060733.4:p.His1303Asn
XM_006712039.2:c.3541C>A	XP_006712102.1:p.His1181Asn
XM_006712040.1:c.3127C>A	XP_006712103.1:p.His1043Asn
XM_011532950.1:c.3904C>A	XP_011531252.1:p.His1302Asn
XM_011532951.1:c.3733C>A	XP_011531253.1:p.His1245Asn
NM_018263.5:c.3907C>A	NP_060733.4:p.His1303Asn
XM_006712039.3:c.3541C>A	XP_006712102.1:p.His1181Asn
XM_006712040.2:c.3127C>A	XP_006712103.1:p.His1043Asn
XM_011532950.3:c.3904C>A	XP_011531252.1:p.His1302Asn
XM_011532951.2:c.3733C>A	XP_011531253.1:p.His1245Asn
XM_017004430.1:c.3127C>A	XP_016859919.1:p.His1043Asn
XM_024452974.1:c.4087C>A	XP_024308742.1:p.His1363Asn
NM_001369346.1:c.3733C>A	NP_001356275.1:p.His1245Asn
NM_001369347.1:c.3127C>A	NP_001356276.1:p.His1043Asn
NM_018263.6:c.3907C>A MANE Select	NP_060733.4:p.His1303Asn