Canonical Allele Identifier: CA1929222447
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781886C= , CM000672.2:g.94781886C= GRCh38
NC_000010.10:g.96541643C= , CM000672.1:g.96541643C= GRCh37
NC_000010.9:g.96531633C= NCBI36
NG_008384.2:g.24181C=
NG_008384.3:g.24206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.708C= MANE Select ENSP00000360372.3:p.Asn236=
ENST00000645461.1:n.1761C=
ENST00000371321.7:c.708C= ENSP00000360372.3:p.Asn236=
ENST00000464755.1:c.1471C= ENSP00000483243.1:n.1471C=
NM_000769.2:c.708C= NP_000760.1:p.Asn236=
NM_000769.4:c.708C= MANE Select NP_000760.1:p.Asn236=