Canonical Allele Identifier: CA2576695331
Gene: ASXL2 HGNC NCBI

Linked Data

gnomAD v4: 2-25742017-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.25742017T>C , CM000664.2:g.25742017T>C GRCh38
NC_000002.11:g.25964886T>C , CM000664.1:g.25964886T>C GRCh37
NC_000002.10:g.25818390T>C NCBI36
NG_052995.1:g.141500A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000336112.9:c.*12A>G ENSP00000337250.5:n.*12A>G
ENST00000435504.9:c.*12A>G MANE Select ENSP00000391447.3:n.*12A>G
ENST00000336112.8:c.*12A>G ENSP00000337250.4:n.*12A>G
ENST00000404843.5:c.*12A>G ENSP00000383920.1:n.*12A>G
ENST00000435504.8:c.*12A>G ENSP00000391447.3:n.*12A>G
NM_018263.4:c.*12A>G NP_060733.4:n.*12A>G
XM_006712039.2:c.*12A>G XP_006712102.1:n.*12A>G
XM_006712040.1:c.*12A>G XP_006712103.1:n.*12A>G
XM_011532950.1:c.*12A>G XP_011531252.1:n.*12A>G
XM_011532951.1:c.*12A>G XP_011531253.1:n.*12A>G
NM_018263.5:c.*12A>G NP_060733.4:n.*12A>G
XM_006712039.3:c.*12A>G XP_006712102.1:n.*12A>G
XM_006712040.2:c.*12A>G XP_006712103.1:n.*12A>G
XM_011532950.3:c.*12A>G XP_011531252.1:n.*12A>G
XM_011532951.2:c.*12A>G XP_011531253.1:n.*12A>G
XM_017004430.1:c.*12A>G XP_016859919.1:n.*12A>G
XM_024452974.1:c.*12A>G XP_024308742.1:n.*12A>G
NM_001369346.1:c.*12A>G NP_001356275.1:n.*12A>G
NM_001369347.1:c.*12A>G NP_001356276.1:n.*12A>G
NM_018263.6:c.*12A>G MANE Select NP_060733.4:n.*12A>G