Canonical Allele Identifier: CA434869612
Gene: IMPG2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.100962463G>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.2712C>T MANE Select ENSP00000193391.6:p.Ser904=
ENST00000193391.7:c.2712C>T ENSP00000193391.6:p.Ser904=
NM_016247.3:c.2712C>T NP_057331.2:p.Ser904=
XM_011512871.1:c.2418C>T XP_011511173.1:p.Ser806=
XM_011512872.1:c.2301C>T XP_011511174.1:p.Ser767=
NM_016247.4:c.2712C>T MANE Select NP_057331.2:p.Ser904=
Search 100 bp 5'
Search 100 bp 3'