Canonical Allele Identifier: CA2726247282

Gene: MIP

Linked Data

• dbSNP Id: rs2136163206

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56450140A>C , CM000674.2:g.56450140A>C	GRCh38
NC_000012.11:g.56843924A>C , CM000674.1:g.56843924A>C	GRCh37
NC_000012.10:g.55130191A>C	NCBI36
NG_021397.1:g.9512T>G
NG_021397.2:g.24027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000648304.1:c.*1556T>G	ENSP00000497190.1:n.*1556T>G
ENST00000652304.1:c.*1140T>G MANE Select	ENSP00000498622.1:n.*1140T>G
ENST00000257979.4:c.*1140T>G	ENSP00000257979.4:n.*1140T>G
NM_012064.3:c.*1140T>G	NP_036196.1:n.*1140T>G
XM_011538354.1:c.*1140T>G	XP_011536656.1:n.*1140T>G
NM_012064.4:c.*1140T>G MANE Select	NP_036196.1:n.*1140T>G
XM_017019306.1:c.*1140T>G	XP_016874795.1:n.*1140T>G