Canonical Allele Identifier: CA435766702
Gene: GP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.128780738C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061895C>G , CM000665.2:g.129061895C>G GRCh38
NC_000003.11:g.128780738C>G , CM000665.1:g.128780738C>G GRCh37
NC_000003.10:g.130263428C>G NCBI36
NG_008715.1:g.6094C>G , LRG_477:g.6094C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.156C>G MANE Select ENSP00000303942.4:p.Arg52=
ENST00000307395.4:c.156C>G ENSP00000303942.4:p.Arg52=
NM_000174.4:c.156C>G , LRG_477t1:c.156C>G NP_000165.1:p.Arg52=
XM_005247374.3:c.156C>G XP_005247431.1:p.Arg52=
XM_011512701.1:c.156C>G XP_011511003.1:p.Arg52=
XM_011512702.1:c.156C>G XP_011511004.1:p.Arg52=
NM_000174.5:c.156C>G MANE Select NP_000165.1:p.Arg52=
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Search 100 bp 3'