Canonical Allele Identifier: CA354446809
Gene: GP9 HGNC NCBI

Linked Data

dbSNP Id: rs1576798362
MyVariant Identifiers: chr3:g.128780688G>A (hg19) chr3:g.129061845G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061845G>A , CM000665.2:g.129061845G>A GRCh38
NC_000003.11:g.128780688G>A , CM000665.1:g.128780688G>A GRCh37
NC_000003.10:g.130263378G>A NCBI36
NG_008715.1:g.6044G>A , LRG_477:g.6044G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.106G>A MANE Select ENSP00000303942.4:p.Val36Met
ENST00000307395.4:c.106G>A ENSP00000303942.4:p.Val36Met
NM_000174.4:c.106G>A , LRG_477t1:c.106G>A NP_000165.1:p.Val36Met
XM_005247374.3:c.106G>A XP_005247431.1:p.Val36Met
XM_011512701.1:c.106G>A XP_011511003.1:p.Val36Met
XM_011512702.1:c.106G>A XP_011511004.1:p.Val36Met
NM_000174.5:c.106G>A MANE Select NP_000165.1:p.Val36Met
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