Canonical Allele Identifier: CA2667574716
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061665-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061665C>A , CM000665.2:g.129061665C>A GRCh38
NC_000003.11:g.128780508C>A , CM000665.1:g.128780508C>A GRCh37
NC_000003.10:g.130263198C>A NCBI36
NG_008715.1:g.5864C>A , LRG_477:g.5864C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000307395.5:c.-13+46C>A MANE Select ENSP00000303942.4:n.-13+46C>A
ENST00000307395.4:c.-13+46C>A ENSP00000303942.4:n.-13+46C>A
NM_000174.4:c.-13+46C>A , LRG_477t1:c.-13+46C>A NP_000165.1:n.-13+46C>A
XM_005247374.3:c.-13+46C>A XP_005247431.1:n.-13+46C>A
XM_011512701.1:c.-13+46C>A XP_011511003.1:n.-13+46C>A
XM_011512702.1:c.-12-63C>A XP_011511004.1:n.-12-63C>A
NM_000174.5:c.-13+46C>A MANE Select NP_000165.1:n.-13+46C>A
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