Canonical Allele Identifier: CA11188379
Gene: MEIS1 HGNC NCBI

Linked Data

dbSNP Id: rs11678354
gnomAD v2: 2-66760079-T-A
gnomAD v3: 2-66532947-T-A
gnomAD v4: 2-66532947-T-A
MyVariant Identifiers: chr2:g.66760079T>A (hg19) chr2:g.66532947T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66532947T>A , CM000664.2:g.66532947T>A GRCh38
NC_000002.11:g.66760079T>A , CM000664.1:g.66760079T>A GRCh37
NC_000002.10:g.66613583T>A NCBI36
NG_011467.1:g.102548T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272369.14:c.889-14996T>A MANE Select ENSP00000272369.8:n.889-14996T>A
ENST00000272369.13:c.889-14996T>A ENSP00000272369.8:n.889-14996T>A
ENST00000398506.6:c.883-14996T>A ENSP00000381518.2:n.883-14996T>A
ENST00000409517.5:n.203-14996T>A
ENST00000450027.2:n.344-14996T>A
ENST00000475239.5:n.449-14996T>A
ENST00000488550.5:c.889-14996T>A ENSP00000475161.1:n.889-14996T>A
ENST00000495021.6:c.694-14996T>A ENSP00000440571.1:n.694-14996T>A
ENST00000542964.5:n.322-14996T>A
ENST00000560281.6:c.889-14996T>A ENSP00000454209.1:n.889-14996T>A
ENST00000606455.5:n.343-14996T>A
NM_002398.2:c.889-14996T>A NP_002389.1:n.889-14996T>A
XM_005264321.1:c.937-14996T>A XP_005264378.1:n.937-14996T>A
XM_005264322.1:c.889-14996T>A XP_005264379.1:n.889-14996T>A
XM_005264323.1:c.937-14996T>A XP_005264380.1:n.937-14996T>A
XM_005264324.3:c.694-14996T>A XP_005264381.1:n.694-14996T>A
XM_005264325.3:c.694-14996T>A XP_005264382.1:n.694-14996T>A
XR_244932.1:n.1523-14996T>A
XR_244933.1:n.1523-14996T>A
NM_002398.3:c.889-14996T>A MANE Select NP_002389.1:n.889-14996T>A
Search 100 bp 5'
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