Canonical Allele Identifier: CA1929222972
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782266T= , CM000672.2:g.94782266T= GRCh38
NC_000010.10:g.96542023T= , CM000672.1:g.96542023T= GRCh37
NC_000010.9:g.96532013T= NCBI36
NG_008384.2:g.24561T=
NG_008384.3:g.24586T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+269T= MANE Select ENSP00000360372.3:n.819+269T=
ENST00000645461.1:n.1872+269T=
ENST00000371321.7:c.819+269T= ENSP00000360372.3:n.819+269T=
ENST00000464755.1:c.1582+269T= ENSP00000483243.1:n.1582+269T=
NM_000769.2:c.819+269T= NP_000760.1:n.819+269T=
NM_000769.4:c.819+269T= MANE Select NP_000760.1:n.819+269T=
Search 100 bp 5'
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