Canonical Allele Identifier: CA435591496
Gene: GP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.128780603G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.129061760G>C , CM000665.2:g.129061760G>C GRCh38
NC_000003.11:g.128780603G>C , CM000665.1:g.128780603G>C GRCh37
NC_000003.10:g.130263293G>C NCBI36
NG_008715.1:g.5959G>C , LRG_477:g.5959G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000307395.5:c.21G>C MANE Select ENSP00000303942.4:p.Leu7=
ENST00000307395.4:c.21G>C ENSP00000303942.4:p.Leu7=
NM_000174.4:c.21G>C , LRG_477t1:c.21G>C NP_000165.1:p.Leu7=
XM_005247374.3:c.21G>C XP_005247431.1:p.Leu7=
XM_011512701.1:c.21G>C XP_011511003.1:p.Leu7=
XM_011512702.1:c.21G>C XP_011511004.1:p.Leu7=
NM_000174.5:c.21G>C MANE Select NP_000165.1:p.Leu7=