Canonical Allele Identifier: CA236200
Gene: IMPG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 191183
ClinVar RCV Id: RCV000171369
dbSNP Id: rs786205565

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101319817G>C , CM000665.2:g.101319817G>C GRCh38
NC_000003.11:g.101038661G>C , CM000665.1:g.101038661G>C GRCh37
NC_000003.10:g.102521351G>C NCBI36
NG_028284.1:g.5759C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.101C>G MANE Select ENSP00000193391.6:p.Ser34Cys
ENST00000193391.7:c.101C>G ENSP00000193391.6:p.Ser34Cys
NM_016247.3:c.101C>G NP_057331.2:p.Ser34Cys
XM_011512872.1:c.-311C>G XP_011511174.1:n.-311C>G
NM_016247.4:c.101C>G MANE Select NP_057331.2:p.Ser34Cys