Canonical Allele Identifier: CA1929221593
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780551C= , CM000672.2:g.94780551C= GRCh38
NC_000010.10:g.96540308C= , CM000672.1:g.96540308C= GRCh37
NC_000010.9:g.96530298C= NCBI36
NG_008384.2:g.22846C=
NG_008384.3:g.22871C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.534C= MANE Select ENSP00000360372.3:p.Ile178=
ENST00000645461.1:n.1587C=
ENST00000371321.7:c.534C= ENSP00000360372.3:p.Ile178=
ENST00000464755.1:c.1297C= ENSP00000483243.1:n.1297C=
NM_000769.2:c.534C= NP_000760.1:p.Ile178=
NM_000769.4:c.534C= MANE Select NP_000760.1:p.Ile178=
Search 100 bp 5'
Search 100 bp 3'