Canonical Allele Identifier: CA2602622
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs745621166

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061756C>T , CM000665.2:g.129061756C>T GRCh38
NC_000003.11:g.128780599C>T , CM000665.1:g.128780599C>T GRCh37
NC_000003.10:g.130263289C>T NCBI36
NG_008715.1:g.5955C>T , LRG_477:g.5955C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.17C>T MANE Select ENSP00000303942.4:p.Ala6Val
ENST00000307395.4:c.17C>T ENSP00000303942.4:p.Ala6Val
NM_000174.4:c.17C>T , LRG_477t1:c.17C>T NP_000165.1:p.Ala6Val
XM_005247374.3:c.17C>T XP_005247431.1:p.Ala6Val
XM_011512701.1:c.17C>T XP_011511003.1:p.Ala6Val
XM_011512702.1:c.17C>T XP_011511004.1:p.Ala6Val
NM_000174.5:c.17C>T MANE Select NP_000165.1:p.Ala6Val