Canonical Allele Identifier: CA425181263
Gene: ASXL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.25964937G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742068G>A , CM000664.2:g.25742068G>A GRCh38
NC_000002.11:g.25964937G>A , CM000664.1:g.25964937G>A GRCh37
NC_000002.10:g.25818441G>A NCBI36
NG_052995.1:g.141449C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.4266C>T ENSP00000337250.5:p.Gly1422=
ENST00000435504.9:c.4269C>T MANE Select ENSP00000391447.3:p.Gly1423=
ENST00000336112.8:c.4185C>T ENSP00000337250.4:p.Gly1395=
ENST00000404843.5:c.2718C>T ENSP00000383920.1:p.Gly906=
ENST00000435504.8:c.4269C>T ENSP00000391447.3:p.Gly1423=
NM_018263.4:c.4269C>T NP_060733.4:p.Gly1423=
XM_006712039.2:c.3903C>T XP_006712102.1:p.Gly1301=
XM_006712040.1:c.3489C>T XP_006712103.1:p.Gly1163=
XM_011532950.1:c.4266C>T XP_011531252.1:p.Gly1422=
XM_011532951.1:c.4095C>T XP_011531253.1:p.Gly1365=
NM_018263.5:c.4269C>T NP_060733.4:p.Gly1423=
XM_006712039.3:c.3903C>T XP_006712102.1:p.Gly1301=
XM_006712040.2:c.3489C>T XP_006712103.1:p.Gly1163=
XM_011532950.3:c.4266C>T XP_011531252.1:p.Gly1422=
XM_011532951.2:c.4095C>T XP_011531253.1:p.Gly1365=
XM_017004430.1:c.3489C>T XP_016859919.1:p.Gly1163=
XM_024452974.1:c.4449C>T XP_024308742.1:p.Gly1483=
NM_001369346.1:c.4095C>T NP_001356275.1:p.Gly1365=
NM_001369347.1:c.3489C>T NP_001356276.1:p.Gly1163=
NM_018263.6:c.4269C>T MANE Select NP_060733.4:p.Gly1423=