Canonical Allele Identifier: CA269144010
Gene: MEIS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1568679

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.37057601T>C , CM000677.2:g.37057601T>C GRCh38
NC_000015.9:g.37349802T>C , CM000677.1:g.37349802T>C GRCh37
NC_000015.8:g.35137094T>C NCBI36
NG_029108.1:g.48699A>G

Transcript Alleles

HGVS Amino-acid change
NM_001220482.1:c.755-20642A>G VV NP_001207411.1:p.=
NM_002399.3:c.716-20642A>G VV NP_002390.1:p.=
NM_170674.4:c.755-20642A>G VV NP_733774.1:p.=
NM_170675.4:c.755-20642A>G VV NP_733775.1:p.=
NM_170676.4:c.755-20642A>G VV NP_733776.1:p.=
NM_170677.4:c.755-20642A>G VV NP_733777.1:p.=
NM_172315.2:c.716-20642A>G VV NP_758526.1:p.=
NM_172316.2:c.491-20642A>G VV NP_758527.1:p.=
NR_051953.1:n.1429-20642A>G
XM_006720522.2:c.755-20642A>G XP_006720585.1:p.=
XM_006720523.1:c.752-20642A>G XP_006720586.1:p.=
XM_006720524.1:c.752-20642A>G XP_006720587.1:p.=
XM_006720525.1:c.752-20642A>G XP_006720588.1:p.=
XM_006720526.2:c.491-20642A>G XP_006720589.1:p.=
XM_006720527.2:c.317-20642A>G XP_006720590.1:p.=
XM_006720528.2:c.317-20642A>G XP_006720591.1:p.=
XM_006720529.2:c.317-20642A>G XP_006720592.1:p.=
XM_011521591.1:c.317-20642A>G XP_011519893.1:p.=
XM_006720526.3:c.491-20642A>G XP_006720589.1:p.=
XM_006720527.3:c.317-20642A>G XP_006720590.1:p.=
XM_006720529.3:c.317-20642A>G XP_006720592.1:p.=
XM_011521591.2:c.317-20642A>G XP_011519893.1:p.=
XM_017022205.2:c.491-20642A>G XP_016877694.1:p.=
XM_024449925.1:c.716-20642A>G XP_024305693.1:p.=
XM_024449926.1:c.716-20642A>G XP_024305694.1:p.=
XM_024449927.1:c.716-20642A>G XP_024305695.1:p.=
XM_024449928.1:c.491-20642A>G XP_024305696.1:p.=
XM_024449929.1:c.716-20642A>G XP_024305697.1:p.=
XR_001751290.2:n.1190-20642A>G
XR_002957640.1:n.1143-20642A>G
XR_002957641.1:n.1143-20642A>G
NM_170675.5:c.755-20642A>G VV MANE Preferred NP_733775.1:p.=
ENST00000314177.12:c.755-20642A>G ENSP00000326296.8:p.=
ENST00000338564.9:c.755-20642A>G ENSP00000341400.4:p.=
ENST00000340545.9:c.716-20642A>G ENSP00000339549.5:p.=
ENST00000397620.6:c.491-20642A>G ENSP00000380745.2:p.=
ENST00000397624.7:c.491-20642A>G ENSP00000380749.3:p.=
ENST00000424352.6:c.755-20642A>G ENSP00000404185.2:p.=
ENST00000557796.6:c.716-20642A>G ENSP00000452693.2:p.=
ENST00000559085.5:c.716-20642A>G ENSP00000453390.1:p.=
ENST00000559561.5:c.755-20642A>G ENSP00000453497.1:p.=
ENST00000560570.5:c.*316-20642A>G ENSP00000453481.1:p.=
ENST00000561163.5:n.1075-20642A>G
ENST00000561208.5:c.755-20642A>G ENSP00000453793.1:p.=
ENST00000607277.5:n.332-20642A>G ENSP00000475899.1:p.=