Canonical Allele Identifier: CA10615244
Gene: GP9 HGNC NCBI

Linked Data

ClinVar Variation Id: 343219
ClinVar RCV Id: RCV000311083
dbSNP Id: rs886057963
gnomAD v3: 3-129061616-G-T
gnomAD v4: 3-129061616-G-T
MyVariant Identifiers: chr3:g.128780459G>T (hg19) chr3:g.129061616G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061616G>T , CM000665.2:g.129061616G>T GRCh38
NC_000003.11:g.128780459G>T , CM000665.1:g.128780459G>T GRCh37
NC_000003.10:g.130263149G>T NCBI36
NG_008715.1:g.5815G>T , LRG_477:g.5815G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.-16G>T MANE Select ENSP00000303942.4:n.-16G>T
ENST00000307395.4:c.-16G>T ENSP00000303942.4:n.-16G>T
NM_000174.4:c.-16G>T , LRG_477t1:c.-16G>T NP_000165.1:n.-16G>T
XM_005247374.3:c.-16G>T XP_005247431.1:n.-16G>T
XM_011512701.1:c.-16G>T XP_011511003.1:n.-16G>T
XM_011512702.1:c.-12-112G>T XP_011511004.1:n.-12-112G>T
NM_000174.5:c.-16G>T MANE Select NP_000165.1:n.-16G>T
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