Canonical Allele Identifier: CA1929221642
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780653G= , CM000672.2:g.94780653G= GRCh38
NC_000010.10:g.96540410G= , CM000672.1:g.96540410G= GRCh37
NC_000010.9:g.96530400G= NCBI36
NG_008384.2:g.22948G=
NG_008384.3:g.22973G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.636G= MANE Select ENSP00000360372.3:p.Trp212=
ENST00000645461.1:n.1689G=
ENST00000371321.7:c.636G= ENSP00000360372.3:p.Trp212=
ENST00000464755.1:c.1399G= ENSP00000483243.1:n.1399G=
NM_000769.2:c.636G= NP_000760.1:p.Trp212=
NM_000769.4:c.636G= MANE Select NP_000760.1:p.Trp212=