Canonical Allele Identifier: CA2667574671

Gene: GP9

Linked Data

• gnomAD v4: 3-129061621-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061621T>G , CM000665.2:g.129061621T>G	GRCh38
NC_000003.11:g.128780464T>G , CM000665.1:g.128780464T>G	GRCh37
NC_000003.10:g.130263154T>G	NCBI36
NG_008715.1:g.5820T>G , LRG_477:g.5820T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-13+2T>G MANE Select	ENSP00000303942.4:n.-13+2T>G
ENST00000307395.4:c.-13+2T>G	ENSP00000303942.4:n.-13+2T>G
NM_000174.4:c.-13+2T>G , LRG_477t1:c.-13+2T>G	NP_000165.1:n.-13+2T>G
XM_005247374.3:c.-13+2T>G	XP_005247431.1:n.-13+2T>G
XM_011512701.1:c.-13+2T>G	XP_011511003.1:n.-13+2T>G
XM_011512702.1:c.-12-107T>G	XP_011511004.1:n.-12-107T>G
NM_000174.5:c.-13+2T>G MANE Select	NP_000165.1:n.-13+2T>G