Canonical Allele Identifier: CA1929222607
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781960G= , CM000672.2:g.94781960G= GRCh38
NC_000010.10:g.96541717G= , CM000672.1:g.96541717G= GRCh37
NC_000010.9:g.96531707G= NCBI36
NG_008384.2:g.24255G=
NG_008384.3:g.24280G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.782G= MANE Select ENSP00000360372.3:p.Arg261=
ENST00000645461.1:n.1835G=
ENST00000371321.7:c.782G= ENSP00000360372.3:p.Arg261=
ENST00000464755.1:c.1545G= ENSP00000483243.1:n.1545G=
NM_000769.2:c.782G= NP_000760.1:p.Arg261=
NM_000769.4:c.782G= MANE Select NP_000760.1:p.Arg261=
Search 100 bp 5'
Search 100 bp 3'