Canonical Allele Identifier: CA2667574673
Gene: GP9 HGNC NCBI

Linked Data

gnomAD v4: 3-129061622-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061622G>T , CM000665.2:g.129061622G>T GRCh38
NC_000003.11:g.128780465G>T , CM000665.1:g.128780465G>T GRCh37
NC_000003.10:g.130263155G>T NCBI36
NG_008715.1:g.5821G>T , LRG_477:g.5821G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+3G>T MANE Select ENSP00000303942.4:n.-13+3G>T
ENST00000307395.4:c.-13+3G>T ENSP00000303942.4:n.-13+3G>T
NM_000174.4:c.-13+3G>T , LRG_477t1:c.-13+3G>T NP_000165.1:n.-13+3G>T
XM_005247374.3:c.-13+3G>T XP_005247431.1:n.-13+3G>T
XM_011512701.1:c.-13+3G>T XP_011511003.1:n.-13+3G>T
XM_011512702.1:c.-12-106G>T XP_011511004.1:n.-12-106G>T
NM_000174.5:c.-13+3G>T MANE Select NP_000165.1:n.-13+3G>T
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