Canonical Allele Identifier: CA1031728243
Gene: MEIS1 HGNC NCBI

Linked Data

dbSNP Id: rs1320923689
gnomAD v3: 2-66554365-G-T
gnomAD v4: 2-66554365-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.66554365G>T , CM000664.2:g.66554365G>T GRCh38
NC_000002.11:g.66781497G>T , CM000664.1:g.66781497G>T GRCh37
NC_000002.10:g.66635001G>T NCBI36
NG_011467.1:g.123966G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272369.14:c.965+6346G>T MANE Select ENSP00000272369.8:n.965+6346G>T
ENST00000272369.13:c.965+6346G>T ENSP00000272369.8:n.965+6346G>T
ENST00000398506.6:c.959+6346G>T ENSP00000381518.2:n.959+6346G>T
ENST00000409517.5:n.279+6346G>T
ENST00000450027.2:n.420+6346G>T
ENST00000475239.5:n.525+6346G>T
ENST00000488550.5:c.965+6346G>T ENSP00000475161.1:n.965+6346G>T
ENST00000495021.6:c.770+6346G>T ENSP00000440571.1:n.770+6346G>T
ENST00000542964.5:n.398+6346G>T
ENST00000560281.6:c.965+6346G>T ENSP00000454209.1:n.965+6346G>T
ENST00000606455.5:n.419+6346G>T
NM_002398.2:c.965+6346G>T NP_002389.1:n.965+6346G>T
XM_005264321.1:c.1013+6346G>T XP_005264378.1:n.1013+6346G>T
XM_005264322.1:c.965+6346G>T XP_005264379.1:n.965+6346G>T
XM_005264323.1:c.1013+6346G>T XP_005264380.1:n.1013+6346G>T
XM_005264324.3:c.770+6346G>T XP_005264381.1:n.770+6346G>T
XM_005264325.3:c.770+6346G>T XP_005264382.1:n.770+6346G>T
XR_244932.1:n.1599+6346G>T
XR_244933.1:n.1599+6346G>T
NM_002398.3:c.965+6346G>T MANE Select NP_002389.1:n.965+6346G>T