Canonical Allele Identifier: CA50050617

Gene: MEIS1

Linked Data

• dbSNP Id: rs914421129
• MyVariant Identifiers: chr2:g.66781354A>G (hg19) ; chr2:g.66554222A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66554222A>G , CM000664.2:g.66554222A>G	GRCh38
NC_000002.11:g.66781354A>G , CM000664.1:g.66781354A>G	GRCh37
NC_000002.10:g.66634858A>G	NCBI36
NG_011467.1:g.123823A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272369.14:c.965+6203A>G MANE Select	ENSP00000272369.8:n.965+6203A>G
ENST00000272369.13:c.965+6203A>G	ENSP00000272369.8:n.965+6203A>G
ENST00000398506.6:c.959+6203A>G	ENSP00000381518.2:n.959+6203A>G
ENST00000409517.5:n.279+6203A>G
ENST00000450027.2:n.420+6203A>G
ENST00000475239.5:n.525+6203A>G
ENST00000488550.5:c.965+6203A>G	ENSP00000475161.1:n.965+6203A>G
ENST00000495021.6:c.770+6203A>G	ENSP00000440571.1:n.770+6203A>G
ENST00000542964.5:n.398+6203A>G
ENST00000560281.6:c.965+6203A>G	ENSP00000454209.1:n.965+6203A>G
ENST00000606455.5:n.419+6203A>G
NM_002398.2:c.965+6203A>G	NP_002389.1:n.965+6203A>G
XM_005264321.1:c.1013+6203A>G	XP_005264378.1:n.1013+6203A>G
XM_005264322.1:c.965+6203A>G	XP_005264379.1:n.965+6203A>G
XM_005264323.1:c.1013+6203A>G	XP_005264380.1:n.1013+6203A>G
XM_005264324.3:c.770+6203A>G	XP_005264381.1:n.770+6203A>G
XM_005264325.3:c.770+6203A>G	XP_005264382.1:n.770+6203A>G
XR_244932.1:n.1599+6203A>G
XR_244933.1:n.1599+6203A>G
NM_002398.3:c.965+6203A>G MANE Select	NP_002389.1:n.965+6203A>G