Canonical Allele Identifier: CA425354719

Gene: ASXL2

Linked Data

• dbSNP Id: rs1466731921
• gnomAD v2: 2-25965243-G-A
• gnomAD v4: 2-25742374-G-A
• MyVariant Identifiers: chr2:g.25965243G>A (hg19) ; chr2:g.25742374G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742374G>A , CM000664.2:g.25742374G>A	GRCh38
NC_000002.11:g.25965243G>A , CM000664.1:g.25965243G>A	GRCh37
NC_000002.10:g.25818747G>A	NCBI36
NG_052995.1:g.141143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3960C>T	ENSP00000337250.5:p.Thr1320=
ENST00000435504.9:c.3963C>T MANE Select	ENSP00000391447.3:p.Thr1321=
ENST00000336112.8:c.3879C>T	ENSP00000337250.4:p.Thr1293=
ENST00000404843.5:c.2412C>T	ENSP00000383920.1:p.Thr804=
ENST00000435504.8:c.3963C>T	ENSP00000391447.3:p.Thr1321=
NM_018263.4:c.3963C>T	NP_060733.4:p.Thr1321=
XM_006712039.2:c.3597C>T	XP_006712102.1:p.Thr1199=
XM_006712040.1:c.3183C>T	XP_006712103.1:p.Thr1061=
XM_011532950.1:c.3960C>T	XP_011531252.1:p.Thr1320=
XM_011532951.1:c.3789C>T	XP_011531253.1:p.Thr1263=
NM_018263.5:c.3963C>T	NP_060733.4:p.Thr1321=
XM_006712039.3:c.3597C>T	XP_006712102.1:p.Thr1199=
XM_006712040.2:c.3183C>T	XP_006712103.1:p.Thr1061=
XM_011532950.3:c.3960C>T	XP_011531252.1:p.Thr1320=
XM_011532951.2:c.3789C>T	XP_011531253.1:p.Thr1263=
XM_017004430.1:c.3183C>T	XP_016859919.1:p.Thr1061=
XM_024452974.1:c.4143C>T	XP_024308742.1:p.Thr1381=
NM_001369346.1:c.3789C>T	NP_001356275.1:p.Thr1263=
NM_001369347.1:c.3183C>T	NP_001356276.1:p.Thr1061=
NM_018263.6:c.3963C>T MANE Select	NP_060733.4:p.Thr1321=