Canonical Allele Identifier: CA425354739

Gene: ASXL2

Linked Data

• dbSNP Id: rs1485022233
• gnomAD v3: 2-25742380-G-A
• gnomAD v4: 2-25742380-G-A
• MyVariant Identifiers: chr2:g.25965249G>A (hg19) ; chr2:g.25742380G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742380G>A , CM000664.2:g.25742380G>A	GRCh38
NC_000002.11:g.25965249G>A , CM000664.1:g.25965249G>A	GRCh37
NC_000002.10:g.25818753G>A	NCBI36
NG_052995.1:g.141137C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.3954C>T	ENSP00000337250.5:p.Ser1318=
ENST00000435504.9:c.3957C>T MANE Select	ENSP00000391447.3:p.Ser1319=
ENST00000336112.8:c.3873C>T	ENSP00000337250.4:p.Ser1291=
ENST00000404843.5:c.2406C>T	ENSP00000383920.1:p.Ser802=
ENST00000435504.8:c.3957C>T	ENSP00000391447.3:p.Ser1319=
NM_018263.4:c.3957C>T	NP_060733.4:p.Ser1319=
XM_006712039.2:c.3591C>T	XP_006712102.1:p.Ser1197=
XM_006712040.1:c.3177C>T	XP_006712103.1:p.Ser1059=
XM_011532950.1:c.3954C>T	XP_011531252.1:p.Ser1318=
XM_011532951.1:c.3783C>T	XP_011531253.1:p.Ser1261=
NM_018263.5:c.3957C>T	NP_060733.4:p.Ser1319=
XM_006712039.3:c.3591C>T	XP_006712102.1:p.Ser1197=
XM_006712040.2:c.3177C>T	XP_006712103.1:p.Ser1059=
XM_011532950.3:c.3954C>T	XP_011531252.1:p.Ser1318=
XM_011532951.2:c.3783C>T	XP_011531253.1:p.Ser1261=
XM_017004430.1:c.3177C>T	XP_016859919.1:p.Ser1059=
XM_024452974.1:c.4137C>T	XP_024308742.1:p.Ser1379=
NM_001369346.1:c.3783C>T	NP_001356275.1:p.Ser1261=
NM_001369347.1:c.3177C>T	NP_001356276.1:p.Ser1059=
NM_018263.6:c.3957C>T MANE Select	NP_060733.4:p.Ser1319=