Canonical Allele Identifier: CA546191201
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs1274691659
gnomAD v2: 3-128780348-G-A
gnomAD v3: 3-129061505-G-A
gnomAD v4: 3-129061505-G-A
MyVariant Identifiers: chr3:g.128780348G>A (hg19) chr3:g.129061505G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061505G>A , CM000665.2:g.129061505G>A GRCh38
NC_000003.11:g.128780348G>A , CM000665.1:g.128780348G>A GRCh37
NC_000003.10:g.130263038G>A NCBI36
NG_008715.1:g.5704G>A , LRG_477:g.5704G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-127G>A MANE Select ENSP00000303942.4:n.-127G>A
ENST00000307395.4:c.-127G>A ENSP00000303942.4:n.-127G>A
NM_000174.4:c.-127G>A , LRG_477t1:c.-127G>A NP_000165.1:n.-127G>A
XM_005247374.3:c.-127G>A XP_005247431.1:n.-127G>A
XM_011512701.1:c.-127G>A XP_011511003.1:n.-127G>A
XM_011512702.1:c.-12-223G>A XP_011511004.1:n.-12-223G>A
NM_000174.5:c.-127G>A MANE Select NP_000165.1:n.-127G>A
Search 100 bp 5'
Search 100 bp 3'