Canonical Allele Identifier: CA2610265256
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852949-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852949C>A , CM000672.2:g.94852949C>A GRCh38
NC_000010.10:g.96612706C>A , CM000672.1:g.96612706C>A GRCh37
NC_000010.9:g.96602696C>A NCBI36
NG_008384.2:g.95244C>A
NG_008384.3:g.95269C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*35C>A MANE Select ENSP00000360372.3:n.*35C>A
ENST00000645461.1:n.2419C>A
ENST00000371321.7:c.*35C>A ENSP00000360372.3:n.*35C>A
ENST00000464755.1:c.2271C>A ENSP00000483243.1:n.2271C>A
NM_000769.2:c.*35C>A NP_000760.1:n.*35C>A
NM_000769.4:c.*35C>A MANE Select NP_000760.1:n.*35C>A
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