Canonical Allele Identifier: CA2038369948
Gene: MIP HGNC NCBI

Linked Data

dbSNP Id: rs1868546372
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56450220A>G , CM000674.2:g.56450220A>G GRCh38
NC_000012.11:g.56844004A>G , CM000674.1:g.56844004A>G GRCh37
NC_000012.10:g.55130271A>G NCBI36
NG_021397.1:g.9432T>C
NG_021397.2:g.23947T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000648304.1:c.*1476T>C ENSP00000497190.1:n.*1476T>C
ENST00000652304.1:c.*1060T>C MANE Select ENSP00000498622.1:n.*1060T>C
ENST00000257979.4:c.*1060T>C ENSP00000257979.4:n.*1060T>C
NM_012064.3:c.*1060T>C NP_036196.1:n.*1060T>C
XM_011538354.1:c.*1060T>C XP_011536656.1:n.*1060T>C
NM_012064.4:c.*1060T>C MANE Select NP_036196.1:n.*1060T>C
XM_017019306.1:c.*1060T>C XP_016874795.1:n.*1060T>C
Search 100 bp 5'
Search 100 bp 3'