Canonical Allele Identifier: CA50045876

Gene: MEIS1

Linked Data

• dbSNP Id: rs959526394
• gnomAD v3: 2-66531333-T-C
• gnomAD v4: 2-66531333-T-C
• MyVariant Identifiers: chr2:g.66758465T>C (hg19) ; chr2:g.66531333T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.66531333T>C , CM000664.2:g.66531333T>C	GRCh38
NC_000002.11:g.66758465T>C , CM000664.1:g.66758465T>C	GRCh37
NC_000002.10:g.66611969T>C	NCBI36
NG_011467.1:g.100934T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272369.14:c.889-16610T>C MANE Select	ENSP00000272369.8:n.889-16610T>C
ENST00000272369.13:c.889-16610T>C	ENSP00000272369.8:n.889-16610T>C
ENST00000398506.6:c.883-16610T>C	ENSP00000381518.2:n.883-16610T>C
ENST00000409517.5:n.203-16610T>C
ENST00000450027.2:n.344-16610T>C
ENST00000475239.5:n.449-16610T>C
ENST00000488550.5:c.889-16610T>C	ENSP00000475161.1:n.889-16610T>C
ENST00000495021.6:c.694-16610T>C	ENSP00000440571.1:n.694-16610T>C
ENST00000542964.5:n.322-16610T>C
ENST00000560281.6:c.889-16610T>C	ENSP00000454209.1:n.889-16610T>C
ENST00000606455.5:n.343-16610T>C
NM_002398.2:c.889-16610T>C	NP_002389.1:n.889-16610T>C
XM_005264321.1:c.937-16610T>C	XP_005264378.1:n.937-16610T>C
XM_005264322.1:c.889-16610T>C	XP_005264379.1:n.889-16610T>C
XM_005264323.1:c.937-16610T>C	XP_005264380.1:n.937-16610T>C
XM_005264324.3:c.694-16610T>C	XP_005264381.1:n.694-16610T>C
XM_005264325.3:c.694-16610T>C	XP_005264382.1:n.694-16610T>C
XR_244932.1:n.1523-16610T>C
XR_244933.1:n.1523-16610T>C
NM_002398.3:c.889-16610T>C MANE Select	NP_002389.1:n.889-16610T>C