Canonical Allele Identifier: CA346075873
Gene: ASXL2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742521C>G , CM000664.2:g.25742521C>G GRCh38
NC_000002.11:g.25965390C>G , CM000664.1:g.25965390C>G GRCh37
NC_000002.10:g.25818894C>G NCBI36
NG_052995.1:g.140996G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.3813G>C ENSP00000337250.5:p.Gln1271His
ENST00000435504.9:c.3816G>C MANE Select ENSP00000391447.3:p.Gln1272His
ENST00000336112.8:c.3732G>C ENSP00000337250.4:p.Gln1244His
ENST00000404843.5:c.2265G>C ENSP00000383920.1:p.Gln755His
ENST00000435504.8:c.3816G>C ENSP00000391447.3:p.Gln1272His
NM_018263.4:c.3816G>C NP_060733.4:p.Gln1272His
XM_006712039.2:c.3450G>C XP_006712102.1:p.Gln1150His
XM_006712040.1:c.3036G>C XP_006712103.1:p.Gln1012His
XM_011532950.1:c.3813G>C XP_011531252.1:p.Gln1271His
XM_011532951.1:c.3642G>C XP_011531253.1:p.Gln1214His
NM_018263.5:c.3816G>C NP_060733.4:p.Gln1272His
XM_006712039.3:c.3450G>C XP_006712102.1:p.Gln1150His
XM_006712040.2:c.3036G>C XP_006712103.1:p.Gln1012His
XM_011532950.3:c.3813G>C XP_011531252.1:p.Gln1271His
XM_011532951.2:c.3642G>C XP_011531253.1:p.Gln1214His
XM_017004430.1:c.3036G>C XP_016859919.1:p.Gln1012His
XM_024452974.1:c.3996G>C XP_024308742.1:p.Gln1332His
NM_001369346.1:c.3642G>C NP_001356275.1:p.Gln1214His
NM_001369347.1:c.3036G>C NP_001356276.1:p.Gln1012His
NM_018263.6:c.3816G>C MANE Select NP_060733.4:p.Gln1272His