Canonical Allele Identifier: CA255988
Gene: GPC3 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 11689
dbSNP Id: rs104894855

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.133753919G>A , CM000685.2:g.133753919G>A GRCh38
NC_000023.10:g.132887946G>A , CM000685.1:g.132887946G>A GRCh37
NC_000023.9:g.132715612G>A NCBI36
NG_009286.1:g.236721C>T , LRG_505:g.236721C>T

Transcript Alleles

HGVS Amino-acid change
NM_001164617.1:c.595C>T VV NP_001158089.1:p.Arg199Ter
NM_001164618.1:c.547C>T VV NP_001158090.1:p.Arg183Ter
NM_001164619.1:c.433C>T VV NP_001158091.1:p.Arg145Ter
NM_004484.3:c.595C>T , LRG_505t1:c.595C>T NP_004475.1:p.Arg199Ter
XM_017029413.2:c.595C>T XP_016884902.1:p.Arg199Ter
ENST00000370818.7:c.595C>T ENSP00000359854.3:p.Arg199Ter
ENST00000394299.6:c.595C>T ENSP00000377836.2:p.Arg199Ter
ENST00000631057.2:n.433C>T ENSP00000486325.1:p.Arg145Ter