Canonical Allele Identifier: CA11070885
Gene: MEIS1 HGNC NCBI

Linked Data

dbSNP Id: rs12469063
gnomAD v2: 2-66764308-A-G
gnomAD v3: 2-66537176-A-G
gnomAD v4: 2-66537176-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66537176A>G , CM000664.2:g.66537176A>G GRCh38
NC_000002.11:g.66764308A>G , CM000664.1:g.66764308A>G GRCh37
NC_000002.10:g.66617812A>G NCBI36
NG_011467.1:g.106777A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000272369.14:c.889-10767A>G MANE Select ENSP00000272369.8:n.889-10767A>G
ENST00000272369.13:c.889-10767A>G ENSP00000272369.8:n.889-10767A>G
ENST00000398506.6:c.883-10767A>G ENSP00000381518.2:n.883-10767A>G
ENST00000409517.5:n.203-10767A>G
ENST00000450027.2:n.344-10767A>G
ENST00000475239.5:n.449-10767A>G
ENST00000488550.5:c.889-10767A>G ENSP00000475161.1:n.889-10767A>G
ENST00000495021.6:c.694-10767A>G ENSP00000440571.1:n.694-10767A>G
ENST00000542964.5:n.322-10767A>G
ENST00000560281.6:c.889-10767A>G ENSP00000454209.1:n.889-10767A>G
ENST00000606455.5:n.343-10767A>G
NM_002398.2:c.889-10767A>G NP_002389.1:n.889-10767A>G
XM_005264321.1:c.937-10767A>G XP_005264378.1:n.937-10767A>G
XM_005264322.1:c.889-10767A>G XP_005264379.1:n.889-10767A>G
XM_005264323.1:c.937-10767A>G XP_005264380.1:n.937-10767A>G
XM_005264324.3:c.694-10767A>G XP_005264381.1:n.694-10767A>G
XM_005264325.3:c.694-10767A>G XP_005264382.1:n.694-10767A>G
XR_244932.1:n.1523-10767A>G
XR_244933.1:n.1523-10767A>G
NM_002398.3:c.889-10767A>G MANE Select NP_002389.1:n.889-10767A>G