Canonical Allele Identifier: CA2667574677
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061626-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061626G>T , CM000665.2:g.129061626G>T GRCh38
NC_000003.11:g.128780469G>T , CM000665.1:g.128780469G>T GRCh37
NC_000003.10:g.130263159G>T NCBI36
NG_008715.1:g.5825G>T , LRG_477:g.5825G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+7G>T MANE Select ENSP00000303942.4:n.-13+7G>T
ENST00000307395.4:c.-13+7G>T ENSP00000303942.4:n.-13+7G>T
NM_000174.4:c.-13+7G>T , LRG_477t1:c.-13+7G>T NP_000165.1:n.-13+7G>T
XM_005247374.3:c.-13+7G>T XP_005247431.1:n.-13+7G>T
XM_011512701.1:c.-13+7G>T XP_011511003.1:n.-13+7G>T
XM_011512702.1:c.-12-102G>T XP_011511004.1:n.-12-102G>T
NM_000174.5:c.-13+7G>T MANE Select NP_000165.1:n.-13+7G>T
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