Canonical Allele Identifier: CA898688334

Gene: GP9

Linked Data

• dbSNP Id: rs1238133832
• gnomAD v3: 3-129061470-A-T
• gnomAD v4: 3-129061470-A-T
• MyVariant Identifiers: chr3:g.128780313A>T (hg19) ; chr3:g.129061470A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061470A>T , CM000665.2:g.129061470A>T	GRCh38
NC_000003.11:g.128780313A>T , CM000665.1:g.128780313A>T	GRCh37
NC_000003.10:g.130263003A>T	NCBI36
NG_008715.1:g.5669A>T , LRG_477:g.5669A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-138-24A>T MANE Select	ENSP00000303942.4:n.-138-24A>T
ENST00000307395.4:c.-138-24A>T	ENSP00000303942.4:n.-138-24A>T
NM_000174.4:c.-138-24A>T , LRG_477t1:c.-138-24A>T	NP_000165.1:n.-138-24A>T
XM_005247374.3:c.-138-24A>T	XP_005247431.1:n.-138-24A>T
XM_011512701.1:c.-138-24A>T	XP_011511003.1:n.-138-24A>T
XM_011512702.1:c.-12-258A>T	XP_011511004.1:n.-12-258A>T
NM_000174.5:c.-138-24A>T MANE Select	NP_000165.1:n.-138-24A>T