Canonical Allele Identifier: CA353855907
Gene: IMPG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.100962463G>T (hg19) chr3:g.101243619G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101243619G>T , CM000665.2:g.101243619G>T GRCh38
NC_000003.11:g.100962463G>T , CM000665.1:g.100962463G>T GRCh37
NC_000003.10:g.102445153G>T NCBI36
NG_028284.1:g.81957C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.2712C>A MANE Select ENSP00000193391.6:p.Ser904Arg
ENST00000193391.7:c.2712C>A ENSP00000193391.6:p.Ser904Arg
NM_016247.3:c.2712C>A NP_057331.2:p.Ser904Arg
XM_011512871.1:c.2418C>A XP_011511173.1:p.Ser806Arg
XM_011512872.1:c.2301C>A XP_011511174.1:p.Ser767Arg
NM_016247.4:c.2712C>A MANE Select NP_057331.2:p.Ser904Arg
Search 100 bp 5'
Search 100 bp 3'