Canonical Allele Identifier: CA435766836

Gene: GP9

Linked Data

• MyVariant Identifiers: chr3:g.128780786G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061943G>T , CM000665.2:g.129061943G>T	GRCh38
NC_000003.11:g.128780786G>T , CM000665.1:g.128780786G>T	GRCh37
NC_000003.10:g.130263476G>T	NCBI36
NG_008715.1:g.6142G>T , LRG_477:g.6142G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.204G>T MANE Select	ENSP00000303942.4:p.Pro68=
ENST00000307395.4:c.204G>T	ENSP00000303942.4:p.Pro68=
NM_000174.4:c.204G>T , LRG_477t1:c.204G>T	NP_000165.1:p.Pro68=
XM_005247374.3:c.204G>T	XP_005247431.1:p.Pro68=
XM_011512701.1:c.204G>T	XP_011511003.1:p.Pro68=
XM_011512702.1:c.204G>T	XP_011511004.1:p.Pro68=
NM_000174.5:c.204G>T MANE Select	NP_000165.1:p.Pro68=