Canonical Allele Identifier: CA898688496

Gene: GP9

Linked Data

• dbSNP Id: rs1348575674
• gnomAD v3: 3-129061652-T-C
• gnomAD v4: 3-129061652-T-C
• MyVariant Identifiers: chr3:g.128780495T>C (hg19) ; chr3:g.129061652T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061652T>C , CM000665.2:g.129061652T>C	GRCh38
NC_000003.11:g.128780495T>C , CM000665.1:g.128780495T>C	GRCh37
NC_000003.10:g.130263185T>C	NCBI36
NG_008715.1:g.5851T>C , LRG_477:g.5851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-13+33T>C MANE Select	ENSP00000303942.4:n.-13+33T>C
ENST00000307395.4:c.-13+33T>C	ENSP00000303942.4:n.-13+33T>C
NM_000174.4:c.-13+33T>C , LRG_477t1:c.-13+33T>C	NP_000165.1:n.-13+33T>C
XM_005247374.3:c.-13+33T>C	XP_005247431.1:n.-13+33T>C
XM_011512701.1:c.-13+33T>C	XP_011511003.1:n.-13+33T>C
XM_011512702.1:c.-12-76T>C	XP_011511004.1:n.-12-76T>C
NM_000174.5:c.-13+33T>C MANE Select	NP_000165.1:n.-13+33T>C