Canonical Allele Identifier: CA1929218699
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775312A= , CM000672.2:g.94775312A= GRCh38
NC_000010.10:g.96535069A= , CM000672.1:g.96535069A= GRCh37
NC_000010.9:g.96525059A= NCBI36
NG_008384.2:g.17607A=
NG_008384.3:g.17632A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.332-78A= MANE Select ENSP00000360372.3:n.332-78A=
ENST00000645461.1:n.1385-78A=
ENST00000371321.7:c.332-78A= ENSP00000360372.3:n.332-78A=
ENST00000464755.1:c.1095-78A= ENSP00000483243.1:n.1095-78A=
ENST00000480405.2:c.332-78A= ENSP00000483847.1:n.332-78A=
NM_000769.2:c.332-78A= NP_000760.1:n.332-78A=
NM_000769.4:c.332-78A= MANE Select NP_000760.1:n.332-78A=