Canonical Allele Identifier: CA546191213
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs1361131831
gnomAD v2: 3-128780505-G-A
gnomAD v3: 3-129061662-G-A
gnomAD v4: 3-129061662-G-A
MyVariant Identifiers: chr3:g.128780505G>A (hg19) chr3:g.129061662G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061662G>A , CM000665.2:g.129061662G>A GRCh38
NC_000003.11:g.128780505G>A , CM000665.1:g.128780505G>A GRCh37
NC_000003.10:g.130263195G>A NCBI36
NG_008715.1:g.5861G>A , LRG_477:g.5861G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-13+43G>A MANE Select ENSP00000303942.4:n.-13+43G>A
ENST00000307395.4:c.-13+43G>A ENSP00000303942.4:n.-13+43G>A
NM_000174.4:c.-13+43G>A , LRG_477t1:c.-13+43G>A NP_000165.1:n.-13+43G>A
XM_005247374.3:c.-13+43G>A XP_005247431.1:n.-13+43G>A
XM_011512701.1:c.-13+43G>A XP_011511003.1:n.-13+43G>A
XM_011512702.1:c.-12-66G>A XP_011511004.1:n.-12-66G>A
NM_000174.5:c.-13+43G>A MANE Select NP_000165.1:n.-13+43G>A
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