Canonical Allele Identifier: CA354446425

Gene: GP9

Linked Data

• MyVariant Identifiers: chr3:g.128780619A>T (hg19) ; chr3:g.129061776A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061776A>T , CM000665.2:g.129061776A>T	GRCh38
NC_000003.11:g.128780619A>T , CM000665.1:g.128780619A>T	GRCh37
NC_000003.10:g.130263309A>T	NCBI36
NG_008715.1:g.5975A>T , LRG_477:g.5975A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.37A>T MANE Select	ENSP00000303942.4:p.Thr13Ser
ENST00000307395.4:c.37A>T	ENSP00000303942.4:p.Thr13Ser
NM_000174.4:c.37A>T , LRG_477t1:c.37A>T	NP_000165.1:p.Thr13Ser
XM_005247374.3:c.37A>T	XP_005247431.1:p.Thr13Ser
XM_011512701.1:c.37A>T	XP_011511003.1:p.Thr13Ser
XM_011512702.1:c.37A>T	XP_011511004.1:p.Thr13Ser
NM_000174.5:c.37A>T MANE Select	NP_000165.1:p.Thr13Ser