Canonical Allele Identifier: CA1929222353
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781840C= , CM000672.2:g.94781840C= GRCh38
NC_000010.10:g.96541597C= , CM000672.1:g.96541597C= GRCh37
NC_000010.9:g.96531587C= NCBI36
NG_008384.2:g.24135C=
NG_008384.3:g.24160C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.662C= MANE Select ENSP00000360372.3:p.Thr221=
ENST00000645461.1:n.1715C=
ENST00000371321.7:c.662C= ENSP00000360372.3:p.Thr221=
ENST00000464755.1:c.1425C= ENSP00000483243.1:n.1425C=
NM_000769.2:c.662C= NP_000760.1:p.Thr221=
NM_000769.4:c.662C= MANE Select NP_000760.1:p.Thr221=
Search 100 bp 5'
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