Canonical Allele Identifier: CA354447136
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs1358824218

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061896A>C , CM000665.2:g.129061896A>C GRCh38
NC_000003.11:g.128780739A>C , CM000665.1:g.128780739A>C GRCh37
NC_000003.10:g.130263429A>C NCBI36
NG_008715.1:g.6095A>C , LRG_477:g.6095A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.157A>C MANE Select ENSP00000303942.4:p.Thr53Pro
ENST00000307395.4:c.157A>C ENSP00000303942.4:p.Thr53Pro
NM_000174.4:c.157A>C , LRG_477t1:c.157A>C NP_000165.1:p.Thr53Pro
XM_005247374.3:c.157A>C XP_005247431.1:p.Thr53Pro
XM_011512701.1:c.157A>C XP_011511003.1:p.Thr53Pro
XM_011512702.1:c.157A>C XP_011511004.1:p.Thr53Pro
NM_000174.5:c.157A>C MANE Select NP_000165.1:p.Thr53Pro