Canonical Allele Identifier: CA1929218752
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775394C= , CM000672.2:g.94775394C= GRCh38
NC_000010.10:g.96535151C= , CM000672.1:g.96535151C= GRCh37
NC_000010.9:g.96525141C= NCBI36
NG_008384.2:g.17689C=
NG_008384.3:g.17714C=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.336C= MANE Select ENSP00000360372.3:p.Ile112=
ENST00000645461.1:n.1389C=
ENST00000371321.7:c.336C= ENSP00000360372.3:p.Ile112=
ENST00000464755.1:c.1099C= ENSP00000483243.1:n.1099C=
ENST00000480405.2:c.336C= ENSP00000483847.1:p.Ile112=
NM_000769.2:c.336C= NP_000760.1:p.Ile112=
NM_000769.4:c.336C= MANE Select NP_000760.1:p.Ile112=