Canonical Allele Identifier: CA353855921
Gene: IMPG2 HGNC NCBI

Linked Data

dbSNP Id: rs1260137025
gnomAD v2: 3-100962465-T-C
gnomAD v4: 3-101243621-T-C
MyVariant Identifiers: chr3:g.100962465T>C (hg19) chr3:g.101243621T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.101243621T>C , CM000665.2:g.101243621T>C GRCh38
NC_000003.11:g.100962465T>C , CM000665.1:g.100962465T>C GRCh37
NC_000003.10:g.102445155T>C NCBI36
NG_028284.1:g.81955A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000193391.8:c.2710A>G MANE Select ENSP00000193391.6:p.Ser904Gly
ENST00000193391.7:c.2710A>G ENSP00000193391.6:p.Ser904Gly
NM_016247.3:c.2710A>G NP_057331.2:p.Ser904Gly
XM_011512871.1:c.2416A>G XP_011511173.1:p.Ser806Gly
XM_011512872.1:c.2299A>G XP_011511174.1:p.Ser767Gly
NM_016247.4:c.2710A>G MANE Select NP_057331.2:p.Ser904Gly
Search 100 bp 5'
Search 100 bp 3'