Canonical Allele Identifier: CA2667574721
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061671-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061671G>C , CM000665.2:g.129061671G>C GRCh38
NC_000003.11:g.128780514G>C , CM000665.1:g.128780514G>C GRCh37
NC_000003.10:g.130263204G>C NCBI36
NG_008715.1:g.5870G>C , LRG_477:g.5870G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+52G>C MANE Select ENSP00000303942.4:n.-13+52G>C
ENST00000307395.4:c.-13+52G>C ENSP00000303942.4:n.-13+52G>C
NM_000174.4:c.-13+52G>C , LRG_477t1:c.-13+52G>C NP_000165.1:n.-13+52G>C
XM_005247374.3:c.-13+52G>C XP_005247431.1:n.-13+52G>C
XM_011512701.1:c.-13+52G>C XP_011511003.1:n.-13+52G>C
XM_011512702.1:c.-12-57G>C XP_011511004.1:n.-12-57G>C
NM_000174.5:c.-13+52G>C MANE Select NP_000165.1:n.-13+52G>C
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