Canonical Allele Identifier: CA1929278275
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849977C= , CM000672.2:g.94849977C= GRCh38
NC_000010.10:g.96609734C= , CM000672.1:g.96609734C= GRCh37
NC_000010.9:g.96599724C= NCBI36
NG_008384.2:g.92272C=
NG_008384.3:g.92297C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1210C= MANE Select ENSP00000360372.3:p.Pro404=
ENST00000645461.1:n.2121C=
ENST00000371321.7:c.1210C= ENSP00000360372.3:p.Pro404=
ENST00000464755.1:c.1973C= ENSP00000483243.1:n.1973C=
NM_000769.2:c.1210C= NP_000760.1:p.Pro404=
NM_000769.4:c.1210C= MANE Select NP_000760.1:p.Pro404=