Canonical Allele Identifier: CA2581900795

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061508C>A , CM000665.2:g.129061508C>A	GRCh38
NC_000003.11:g.128780351C>A , CM000665.1:g.128780351C>A	GRCh37
NC_000003.10:g.130263041C>A	NCBI36
NG_008715.1:g.5707C>A , LRG_477:g.5707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.-124C>A MANE Select	ENSP00000303942.4:n.-124C>A
ENST00000307395.4:c.-124C>A	ENSP00000303942.4:n.-124C>A
NM_000174.4:c.-124C>A , LRG_477t1:c.-124C>A	NP_000165.1:n.-124C>A
XM_005247374.3:c.-124C>A	XP_005247431.1:n.-124C>A
XM_011512701.1:c.-124C>A	XP_011511003.1:n.-124C>A
XM_011512702.1:c.-12-220C>A	XP_011511004.1:n.-12-220C>A
NM_000174.5:c.-124C>A MANE Select	NP_000165.1:n.-124C>A