Canonical Allele Identifier: CA1400981613

Gene: GP9

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061894G= , CM000665.2:g.129061894G=	GRCh38
NC_000003.11:g.128780737G= , CM000665.1:g.128780737G=	GRCh37
NC_000003.10:g.130263427G=	NCBI36
NG_008715.1:g.6093G= , LRG_477:g.6093G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.155G= MANE Select	ENSP00000303942.4:p.Arg52=
ENST00000307395.4:c.155G=	ENSP00000303942.4:p.Arg52=
NM_000174.4:c.155G= , LRG_477t1:c.155G=	NP_000165.1:p.Arg52=
XM_005247374.3:c.155G=	XP_005247431.1:p.Arg52=
XM_011512701.1:c.155G=	XP_011511003.1:p.Arg52=
XM_011512702.1:c.155G=	XP_011511004.1:p.Arg52=
NM_000174.5:c.155G= MANE Select	NP_000165.1:p.Arg52=