Canonical Allele Identifier: CA2610264898
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94782083-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782083A>G , CM000672.2:g.94782083A>G GRCh38
NC_000010.10:g.96541840A>G , CM000672.1:g.96541840A>G GRCh37
NC_000010.9:g.96531830A>G NCBI36
NG_008384.2:g.24378A>G
NG_008384.3:g.24403A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+86A>G MANE Select ENSP00000360372.3:n.819+86A>G
ENST00000645461.1:n.1872+86A>G
ENST00000371321.7:c.819+86A>G ENSP00000360372.3:n.819+86A>G
ENST00000464755.1:c.1582+86A>G ENSP00000483243.1:n.1582+86A>G
NM_000769.2:c.819+86A>G NP_000760.1:n.819+86A>G
NM_000769.4:c.819+86A>G MANE Select NP_000760.1:n.819+86A>G
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