Canonical Allele Identifier: CA2602643
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs550480973
ExAC: 3:128780732 G / C
gnomAD v2: 3-128780732-G-C
gnomAD v4: 3-129061889-G-C
MyVariant Identifiers: chr3:g.128780732G>C (hg19) chr3:g.129061889G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061889G>C , CM000665.2:g.129061889G>C GRCh38
NC_000003.11:g.128780732G>C , CM000665.1:g.128780732G>C GRCh37
NC_000003.10:g.130263422G>C NCBI36
NG_008715.1:g.6088G>C , LRG_477:g.6088G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.150G>C MANE Select ENSP00000303942.4:p.Pro50=
ENST00000307395.4:c.150G>C ENSP00000303942.4:p.Pro50=
NM_000174.4:c.150G>C , LRG_477t1:c.150G>C NP_000165.1:p.Pro50=
XM_005247374.3:c.150G>C XP_005247431.1:p.Pro50=
XM_011512701.1:c.150G>C XP_011511003.1:p.Pro50=
XM_011512702.1:c.150G>C XP_011511004.1:p.Pro50=
NM_000174.5:c.150G>C MANE Select NP_000165.1:p.Pro50=
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