Canonical Allele Identifier: CA435766728
Gene: GP9 HGNC NCBI

Linked Data

COSMIC: COSM5559760
MyVariant Identifiers: chr3:g.128780750T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061907T>C , CM000665.2:g.129061907T>C GRCh38
NC_000003.11:g.128780750T>C , CM000665.1:g.128780750T>C GRCh37
NC_000003.10:g.130263440T>C NCBI36
NG_008715.1:g.6106T>C , LRG_477:g.6106T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.168T>C MANE Select ENSP00000303942.4:p.Leu56=
ENST00000307395.4:c.168T>C ENSP00000303942.4:p.Leu56=
NM_000174.4:c.168T>C , LRG_477t1:c.168T>C NP_000165.1:p.Leu56=
XM_005247374.3:c.168T>C XP_005247431.1:p.Leu56=
XM_011512701.1:c.168T>C XP_011511003.1:p.Leu56=
XM_011512702.1:c.168T>C XP_011511004.1:p.Leu56=
NM_000174.5:c.168T>C MANE Select NP_000165.1:p.Leu56=
Search 100 bp 5'
Search 100 bp 3'