Canonical Allele Identifier: CA435766766

Gene: GP9

Linked Data

• MyVariant Identifiers: chr3:g.128780765C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061922C>T , CM000665.2:g.129061922C>T	GRCh38
NC_000003.11:g.128780765C>T , CM000665.1:g.128780765C>T	GRCh37
NC_000003.10:g.130263455C>T	NCBI36
NG_008715.1:g.6121C>T , LRG_477:g.6121C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.183C>T MANE Select	ENSP00000303942.4:p.Asn61=
ENST00000307395.4:c.183C>T	ENSP00000303942.4:p.Asn61=
NM_000174.4:c.183C>T , LRG_477t1:c.183C>T	NP_000165.1:p.Asn61=
XM_005247374.3:c.183C>T	XP_005247431.1:p.Asn61=
XM_011512701.1:c.183C>T	XP_011511003.1:p.Asn61=
XM_011512702.1:c.183C>T	XP_011511004.1:p.Asn61=
NM_000174.5:c.183C>T MANE Select	NP_000165.1:p.Asn61=