Canonical Allele Identifier: CA82552398
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 1084639
ClinVar RCV Id: RCV001401714
dbSNP Id: rs923137982
gnomAD v4: 3-129061991-G-A
MyVariant Identifiers: chr3:g.128780834G>A (hg19) chr3:g.129061991G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061991G>A , CM000665.2:g.129061991G>A GRCh38
NC_000003.11:g.128780834G>A , CM000665.1:g.128780834G>A GRCh37
NC_000003.10:g.130263524G>A NCBI36
NG_008715.1:g.6190G>A , LRG_477:g.6190G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.252G>A MANE Select ENSP00000303942.4:p.Gln84=
ENST00000307395.4:c.252G>A ENSP00000303942.4:p.Gln84=
NM_000174.4:c.252G>A , LRG_477t1:c.252G>A NP_000165.1:p.Gln84=
XM_005247374.3:c.252G>A XP_005247431.1:p.Gln84=
XM_011512701.1:c.252G>A XP_011511003.1:p.Gln84=
XM_011512702.1:c.252G>A XP_011511004.1:p.Gln84=
NM_000174.5:c.252G>A MANE Select NP_000165.1:p.Gln84=
Search 100 bp 5'
Search 100 bp 3'