Canonical Allele Identifier: CA2667574714
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061663-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061663T>G , CM000665.2:g.129061663T>G GRCh38
NC_000003.11:g.128780506T>G , CM000665.1:g.128780506T>G GRCh37
NC_000003.10:g.130263196T>G NCBI36
NG_008715.1:g.5862T>G , LRG_477:g.5862T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+44T>G MANE Select ENSP00000303942.4:n.-13+44T>G
ENST00000307395.4:c.-13+44T>G ENSP00000303942.4:n.-13+44T>G
NM_000174.4:c.-13+44T>G , LRG_477t1:c.-13+44T>G NP_000165.1:n.-13+44T>G
XM_005247374.3:c.-13+44T>G XP_005247431.1:n.-13+44T>G
XM_011512701.1:c.-13+44T>G XP_011511003.1:n.-13+44T>G
XM_011512702.1:c.-12-65T>G XP_011511004.1:n.-12-65T>G
NM_000174.5:c.-13+44T>G MANE Select NP_000165.1:n.-13+44T>G
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