Canonical Allele Identifier: CA1557342

Gene: ASXL2

Linked Data

• dbSNP Id: rs762477855
• ExAC: 2:25965029 T / C
• gnomAD v2: 2-25965029-T-C
• gnomAD v4: 2-25742160-T-C
• MyVariant Identifiers: chr2:g.25965029T>C (hg19) ; chr2:g.25742160T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.25742160T>C , CM000664.2:g.25742160T>C	GRCh38
NC_000002.11:g.25965029T>C , CM000664.1:g.25965029T>C	GRCh37
NC_000002.10:g.25818533T>C	NCBI36
NG_052995.1:g.141357A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336112.9:c.4174A>G	ENSP00000337250.5:p.Ile1392Val
ENST00000435504.9:c.4177A>G MANE Select	ENSP00000391447.3:p.Ile1393Val
ENST00000336112.8:c.4093A>G	ENSP00000337250.4:p.Ile1365Val
ENST00000404843.5:c.2626A>G	ENSP00000383920.1:p.Ile876Val
ENST00000435504.8:c.4177A>G	ENSP00000391447.3:p.Ile1393Val
NM_018263.4:c.4177A>G	NP_060733.4:p.Ile1393Val
XM_006712039.2:c.3811A>G	XP_006712102.1:p.Ile1271Val
XM_006712040.1:c.3397A>G	XP_006712103.1:p.Ile1133Val
XM_011532950.1:c.4174A>G	XP_011531252.1:p.Ile1392Val
XM_011532951.1:c.4003A>G	XP_011531253.1:p.Ile1335Val
NM_018263.5:c.4177A>G	NP_060733.4:p.Ile1393Val
XM_006712039.3:c.3811A>G	XP_006712102.1:p.Ile1271Val
XM_006712040.2:c.3397A>G	XP_006712103.1:p.Ile1133Val
XM_011532950.3:c.4174A>G	XP_011531252.1:p.Ile1392Val
XM_011532951.2:c.4003A>G	XP_011531253.1:p.Ile1335Val
XM_017004430.1:c.3397A>G	XP_016859919.1:p.Ile1133Val
XM_024452974.1:c.4357A>G	XP_024308742.1:p.Ile1453Val
NM_001369346.1:c.4003A>G	NP_001356275.1:p.Ile1335Val
NM_001369347.1:c.3397A>G	NP_001356276.1:p.Ile1133Val
NM_018263.6:c.4177A>G MANE Select	NP_060733.4:p.Ile1393Val