Canonical Allele Identifier: CA82552297

Gene: GP9

Linked Data

• dbSNP Id: rs921030356
• gnomAD v3: 3-129061916-C-T
• gnomAD v4: 3-129061916-C-T
• MyVariant Identifiers: chr3:g.128780759C>T (hg19) ; chr3:g.129061916C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129061916C>T , CM000665.2:g.129061916C>T	GRCh38
NC_000003.11:g.128780759C>T , CM000665.1:g.128780759C>T	GRCh37
NC_000003.10:g.130263449C>T	NCBI36
NG_008715.1:g.6115C>T , LRG_477:g.6115C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307395.5:c.177C>T MANE Select	ENSP00000303942.4:p.Ala59=
ENST00000307395.4:c.177C>T	ENSP00000303942.4:p.Ala59=
NM_000174.4:c.177C>T , LRG_477t1:c.177C>T	NP_000165.1:p.Ala59=
XM_005247374.3:c.177C>T	XP_005247431.1:p.Ala59=
XM_011512701.1:c.177C>T	XP_011511003.1:p.Ala59=
XM_011512702.1:c.177C>T	XP_011511004.1:p.Ala59=
NM_000174.5:c.177C>T MANE Select	NP_000165.1:p.Ala59=