Canonical Allele Identifier: CA2602660
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs758119211
ExAC: 3:128780781 C / A
gnomAD v2: 3-128780781-C-A
gnomAD v4: 3-129061938-C-A
MyVariant Identifiers: chr3:g.128780781C>A (hg19) chr3:g.129061938C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061938C>A , CM000665.2:g.129061938C>A GRCh38
NC_000003.11:g.128780781C>A , CM000665.1:g.128780781C>A GRCh37
NC_000003.10:g.130263471C>A NCBI36
NG_008715.1:g.6137C>A , LRG_477:g.6137C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.199C>A MANE Select ENSP00000303942.4:p.Pro67Thr
ENST00000307395.4:c.199C>A ENSP00000303942.4:p.Pro67Thr
NM_000174.4:c.199C>A , LRG_477t1:c.199C>A NP_000165.1:p.Pro67Thr
XM_005247374.3:c.199C>A XP_005247431.1:p.Pro67Thr
XM_011512701.1:c.199C>A XP_011511003.1:p.Pro67Thr
XM_011512702.1:c.199C>A XP_011511004.1:p.Pro67Thr
NM_000174.5:c.199C>A MANE Select NP_000165.1:p.Pro67Thr
Search 100 bp 5'
Search 100 bp 3'