Canonical Allele Identifier: CA15189087
Gene: MEIS1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6710341

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66531290A>G , CM000664.2:g.66531290A>G GRCh38
NC_000002.11:g.66758422A>G , CM000664.1:g.66758422A>G GRCh37
NC_000002.10:g.66611926A>G NCBI36
NG_011467.1:g.100891A>G

Transcript Alleles

HGVS Amino-acid change
NM_002398.2:c.889-16653A>G VV NP_002389.1:p.=
XM_005264321.1:c.937-16653A>G XP_005264378.1:p.=
XM_005264322.1:c.889-16653A>G XP_005264379.1:p.=
XM_005264323.1:c.937-16653A>G XP_005264380.1:p.=
XM_005264324.3:c.694-16653A>G XP_005264381.1:p.=
XM_005264325.3:c.694-16653A>G XP_005264382.1:p.=
XR_244932.1:n.1523-16653A>G
XR_244933.1:n.1523-16653A>G
NM_002398.3:c.889-16653A>G VV MANE Preferred
ENST00000272369.13:c.889-16653A>G ENSP00000272369.8:p.=
ENST00000398506.6:c.883-16653A>G ENSP00000381518.2:p.=
ENST00000409517.5:n.203-16653A>G
ENST00000450027.2:n.344-16653A>G
ENST00000475239.5:n.449-16653A>G
ENST00000488550.5:c.889-16653A>G ENSP00000475161.1:p.=
ENST00000495021.6:c.694-16653A>G ENSP00000440571.1:p.=
ENST00000542964.5:n.322-16653A>G
ENST00000560281.6:c.889-16653A>G ENSP00000454209.1:p.=
ENST00000606455.5:n.343-16653A>G