Canonical Allele Identifier: CA346074018
Gene: ASXL2 HGNC NCBI

Linked Data

gnomAD v4: 2-25742241-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742241T>C , CM000664.2:g.25742241T>C GRCh38
NC_000002.11:g.25965110T>C , CM000664.1:g.25965110T>C GRCh37
NC_000002.10:g.25818614T>C NCBI36
NG_052995.1:g.141276A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.4093A>G ENSP00000337250.5:p.Thr1365Ala
ENST00000435504.9:c.4096A>G MANE Select ENSP00000391447.3:p.Thr1366Ala
ENST00000336112.8:c.4012A>G ENSP00000337250.4:p.Thr1338Ala
ENST00000404843.5:c.2545A>G ENSP00000383920.1:p.Thr849Ala
ENST00000435504.8:c.4096A>G ENSP00000391447.3:p.Thr1366Ala
NM_018263.4:c.4096A>G NP_060733.4:p.Thr1366Ala
XM_006712039.2:c.3730A>G XP_006712102.1:p.Thr1244Ala
XM_006712040.1:c.3316A>G XP_006712103.1:p.Thr1106Ala
XM_011532950.1:c.4093A>G XP_011531252.1:p.Thr1365Ala
XM_011532951.1:c.3922A>G XP_011531253.1:p.Thr1308Ala
NM_018263.5:c.4096A>G NP_060733.4:p.Thr1366Ala
XM_006712039.3:c.3730A>G XP_006712102.1:p.Thr1244Ala
XM_006712040.2:c.3316A>G XP_006712103.1:p.Thr1106Ala
XM_011532950.3:c.4093A>G XP_011531252.1:p.Thr1365Ala
XM_011532951.2:c.3922A>G XP_011531253.1:p.Thr1308Ala
XM_017004430.1:c.3316A>G XP_016859919.1:p.Thr1106Ala
XM_024452974.1:c.4276A>G XP_024308742.1:p.Thr1426Ala
NM_001369346.1:c.3922A>G NP_001356275.1:p.Thr1308Ala
NM_001369347.1:c.3316A>G NP_001356276.1:p.Thr1106Ala
NM_018263.6:c.4096A>G MANE Select NP_060733.4:p.Thr1366Ala