Canonical Allele Identifier: CA50050568

Gene: MEIS1

Linked Data

• dbSNP Id: rs962672987
• gnomAD v2: 2-66781145-C-T
• gnomAD v3: 2-66554013-C-T
• gnomAD v4: 2-66554013-C-T
• MyVariant Identifiers: chr2:g.66781145C>T (hg19) ; chr2:g.66554013C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66554013C>T , CM000664.2:g.66554013C>T	GRCh38
NC_000002.11:g.66781145C>T , CM000664.1:g.66781145C>T	GRCh37
NC_000002.10:g.66634649C>T	NCBI36
NG_011467.1:g.123614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272369.14:c.965+5994C>T MANE Select	ENSP00000272369.8:n.965+5994C>T
ENST00000272369.13:c.965+5994C>T	ENSP00000272369.8:n.965+5994C>T
ENST00000398506.6:c.959+5994C>T	ENSP00000381518.2:n.959+5994C>T
ENST00000409517.5:n.279+5994C>T
ENST00000450027.2:n.420+5994C>T
ENST00000475239.5:n.525+5994C>T
ENST00000488550.5:c.965+5994C>T	ENSP00000475161.1:n.965+5994C>T
ENST00000495021.6:c.770+5994C>T	ENSP00000440571.1:n.770+5994C>T
ENST00000542964.5:n.398+5994C>T
ENST00000560281.6:c.965+5994C>T	ENSP00000454209.1:n.965+5994C>T
ENST00000606455.5:n.419+5994C>T
NM_002398.2:c.965+5994C>T	NP_002389.1:n.965+5994C>T
XM_005264321.1:c.1013+5994C>T	XP_005264378.1:n.1013+5994C>T
XM_005264322.1:c.965+5994C>T	XP_005264379.1:n.965+5994C>T
XM_005264323.1:c.1013+5994C>T	XP_005264380.1:n.1013+5994C>T
XM_005264324.3:c.770+5994C>T	XP_005264381.1:n.770+5994C>T
XM_005264325.3:c.770+5994C>T	XP_005264382.1:n.770+5994C>T
XR_244932.1:n.1599+5994C>T
XR_244933.1:n.1599+5994C>T
NM_002398.3:c.965+5994C>T MANE Select	NP_002389.1:n.965+5994C>T