Canonical Allele Identifier: CA2604296200
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs2107956283
gnomAD v3: 3-129061657-C-G
gnomAD v4: 3-129061657-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061657C>G , CM000665.2:g.129061657C>G GRCh38
NC_000003.11:g.128780500C>G , CM000665.1:g.128780500C>G GRCh37
NC_000003.10:g.130263190C>G NCBI36
NG_008715.1:g.5856C>G , LRG_477:g.5856C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+38C>G MANE Select ENSP00000303942.4:n.-13+38C>G
ENST00000307395.4:c.-13+38C>G ENSP00000303942.4:n.-13+38C>G
NM_000174.4:c.-13+38C>G , LRG_477t1:c.-13+38C>G NP_000165.1:n.-13+38C>G
XM_005247374.3:c.-13+38C>G XP_005247431.1:n.-13+38C>G
XM_011512701.1:c.-13+38C>G XP_011511003.1:n.-13+38C>G
XM_011512702.1:c.-12-71C>G XP_011511004.1:n.-12-71C>G
NM_000174.5:c.-13+38C>G MANE Select NP_000165.1:n.-13+38C>G
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