Canonical Allele Identifier: CA1929278238
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849923A= , CM000672.2:g.94849923A= GRCh38
NC_000010.10:g.96609680A= , CM000672.1:g.96609680A= GRCh37
NC_000010.9:g.96599670A= NCBI36
NG_008384.2:g.92218A=
NG_008384.3:g.92243A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1156A= MANE Select ENSP00000360372.3:p.Thr386=
ENST00000645461.1:n.2067A=
ENST00000371321.7:c.1156A= ENSP00000360372.3:p.Thr386=
ENST00000464755.1:c.1919A= ENSP00000483243.1:n.1919A=
NM_000769.2:c.1156A= NP_000760.1:p.Thr386=
NM_000769.4:c.1156A= MANE Select NP_000760.1:p.Thr386=