Canonical Allele Identifier: CA2667574713
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061660-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061660C>T , CM000665.2:g.129061660C>T GRCh38
NC_000003.11:g.128780503C>T , CM000665.1:g.128780503C>T GRCh37
NC_000003.10:g.130263193C>T NCBI36
NG_008715.1:g.5859C>T , LRG_477:g.5859C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000307395.5:c.-13+41C>T MANE Select ENSP00000303942.4:n.-13+41C>T
ENST00000307395.4:c.-13+41C>T ENSP00000303942.4:n.-13+41C>T
NM_000174.4:c.-13+41C>T , LRG_477t1:c.-13+41C>T NP_000165.1:n.-13+41C>T
XM_005247374.3:c.-13+41C>T XP_005247431.1:n.-13+41C>T
XM_011512701.1:c.-13+41C>T XP_011511003.1:n.-13+41C>T
XM_011512702.1:c.-12-68C>T XP_011511004.1:n.-12-68C>T
NM_000174.5:c.-13+41C>T MANE Select NP_000165.1:n.-13+41C>T
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