Canonical Allele Identifier: CA1929278274
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849976C= , CM000672.2:g.94849976C= GRCh38
NC_000010.10:g.96609733C= , CM000672.1:g.96609733C= GRCh37
NC_000010.9:g.96599723C= NCBI36
NG_008384.2:g.92271C=
NG_008384.3:g.92296C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1209C= MANE Select ENSP00000360372.3:p.Asn403=
ENST00000645461.1:n.2120C=
ENST00000371321.7:c.1209C= ENSP00000360372.3:p.Asn403=
ENST00000464755.1:c.1972C= ENSP00000483243.1:n.1972C=
NM_000769.2:c.1209C= NP_000760.1:p.Asn403=
NM_000769.4:c.1209C= MANE Select NP_000760.1:p.Asn403=