Canonical Allele Identifier: CA123175
Gene: GP9 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13530
ClinVar RCV Id: RCV000014485
dbSNP Id: rs121918036

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061849A>G , CM000665.2:g.129061849A>G GRCh38
NC_000003.10:g.130263382A>G NCBI36
NC_000003.11:g.128780692A>G , CM000665.1:g.128780692A>G GRCh37
NG_008715.1:g.6048A>G , LRG_477:g.6048A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000307395.4:c.110A>G ENSP00000303942.4:p.Asp37Gly
NM_000174.4:c.110A>G , LRG_477t1:c.110A>G NP_000165.1:p.Asp37Gly
XM_005247374.3:c.110A>G XP_005247431.1:p.Asp37Gly
XM_011512701.1:c.110A>G XP_011511003.1:p.Asp37Gly
XM_011512702.1:c.110A>G XP_011511004.1:p.Asp37Gly