Canonical Allele Identifier: CA434869613
Gene: IMPG2 HGNC NCBI

Linked Data

gnomAD v4: 3-101243622-G-A
MyVariant Identifiers: chr3:g.100962466G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101243622G>A , CM000665.2:g.101243622G>A GRCh38
NC_000003.11:g.100962466G>A , CM000665.1:g.100962466G>A GRCh37
NC_000003.10:g.102445156G>A NCBI36
NG_028284.1:g.81954C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.2709C>T MANE Select ENSP00000193391.6:p.Phe903=
ENST00000193391.7:c.2709C>T ENSP00000193391.6:p.Phe903=
NM_016247.3:c.2709C>T NP_057331.2:p.Phe903=
XM_011512871.1:c.2415C>T XP_011511173.1:p.Phe805=
XM_011512872.1:c.2298C>T XP_011511174.1:p.Phe766=
NM_016247.4:c.2709C>T MANE Select NP_057331.2:p.Phe903=
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