Canonical Allele Identifier: CA2610263937
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775413_94775416del , CM000672.2:g.94775413_94775416del GRCh38
NC_000010.10:g.96535170_96535173del , CM000672.1:g.96535170_96535173del GRCh37
NC_000010.9:g.96525160_96525163del NCBI36
NG_008384.2:g.17708_17711del
NG_008384.3:g.17733_17736del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.355_358del MANE Select ENSP00000360372.3:p.Arg119GlyfsTer10
ENST00000645461.1:n.1408_1411del
ENST00000371321.7:c.355_358del ENSP00000360372.3:p.Arg119GlyfsTer10
ENST00000464755.1:c.1118_1121del ENSP00000483243.1:n.1118_1121del
ENST00000480405.2:c.355_358del ENSP00000483847.1:p.Arg119GlyfsTer10
NM_000769.2:c.355_358del NP_000760.1:p.Arg119GlyfsTer10
NM_000769.4:c.355_358del MANE Select NP_000760.1:p.Arg119GlyfsTer10