Canonical Allele Identifier: CA1929221502
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780376T= , CM000672.2:g.94780376T= GRCh38
NC_000010.10:g.96540133T= , CM000672.1:g.96540133T= GRCh37
NC_000010.9:g.96530123T= NCBI36
NG_008384.2:g.22671T=
NG_008384.3:g.22696T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-123T= MANE Select ENSP00000360372.3:n.482-123T=
ENST00000645461.1:n.1535-123T=
ENST00000371321.7:c.482-123T= ENSP00000360372.3:n.482-123T=
ENST00000464755.1:c.1245-123T= ENSP00000483243.1:n.1245-123T=
NM_000769.2:c.482-123T= NP_000760.1:n.482-123T=
NM_000769.4:c.482-123T= MANE Select NP_000760.1:n.482-123T=