Canonical Allele Identifier: CA236194
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191180
dbSNP Id: rs786205564

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101244057C>T , CM000665.2:g.101244057C>T GRCh38
NC_000003.11:g.100962901C>T , CM000665.1:g.100962901C>T GRCh37
NC_000003.10:g.102445591C>T NCBI36
NG_028284.1:g.81519G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000193391.8:c.2274G>A MANE Select ENSP00000193391.6:p.Trp758Ter
ENST00000193391.7:c.2274G>A ENSP00000193391.6:p.Trp758Ter
NM_016247.3:c.2274G>A NP_057331.2:p.Trp758Ter
XM_011512871.1:c.1980G>A XP_011511173.1:p.Trp660Ter
XM_011512872.1:c.1863G>A XP_011511174.1:p.Trp621Ter
NM_016247.4:c.2274G>A MANE Select NP_057331.2:p.Trp758Ter