Canonical Allele Identifier: CA898688422
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs1379917077
gnomAD v3: 3-129061542-GC-G
gnomAD v4: 3-129061542-GC-G
MyVariant Identifiers: chr3:g.128780386del (hg19) chr3:g.129061543del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061544del , CM000665.2:g.129061544del GRCh38
NC_000003.11:g.128780387del , CM000665.1:g.128780387del GRCh37
NC_000003.10:g.130263077del NCBI36
NG_008715.1:g.5743del , LRG_477:g.5743del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-88del MANE Select ENSP00000303942.4:n.-88del
ENST00000307395.4:c.-88del ENSP00000303942.4:n.-88del
NM_000174.4:c.-88del , LRG_477t1:c.-88del NP_000165.1:n.-88del
XM_005247374.3:c.-88del XP_005247431.1:n.-88del
XM_011512701.1:c.-88del XP_011511003.1:n.-88del
XM_011512702.1:c.-12-184del XP_011511004.1:n.-12-184del
NM_000174.5:c.-88del MANE Select NP_000165.1:n.-88del
Search 100 bp 5'
Search 100 bp 3'