Canonical Allele Identifier: CA353855930
Gene: IMPG2 HGNC NCBI

Linked Data

gnomAD v4: 3-101243623-A-C
MyVariant Identifiers: chr3:g.100962467A>C (hg19) chr3:g.101243623A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101243623A>C , CM000665.2:g.101243623A>C GRCh38
NC_000003.11:g.100962467A>C , CM000665.1:g.100962467A>C GRCh37
NC_000003.10:g.102445157A>C NCBI36
NG_028284.1:g.81953T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.2708T>G MANE Select ENSP00000193391.6:p.Phe903Cys
ENST00000193391.7:c.2708T>G ENSP00000193391.6:p.Phe903Cys
NM_016247.3:c.2708T>G NP_057331.2:p.Phe903Cys
XM_011512871.1:c.2414T>G XP_011511173.1:p.Phe805Cys
XM_011512872.1:c.2297T>G XP_011511174.1:p.Phe766Cys
NM_016247.4:c.2708T>G MANE Select NP_057331.2:p.Phe903Cys
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