Canonical Allele Identifier: CA2610265332
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853051-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853051A>G , CM000672.2:g.94853051A>G GRCh38
NC_000010.10:g.96612808A>G , CM000672.1:g.96612808A>G GRCh37
NC_000010.9:g.96602798A>G NCBI36
NG_008384.2:g.95346A>G
NG_008384.3:g.95371A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*137A>G MANE Select ENSP00000360372.3:n.*137A>G
ENST00000645461.1:n.2521A>G
ENST00000371321.7:c.*137A>G ENSP00000360372.3:n.*137A>G
ENST00000464755.1:c.2373A>G ENSP00000483243.1:n.2373A>G
NM_000769.2:c.*137A>G NP_000760.1:n.*137A>G
NM_000769.4:c.*137A>G MANE Select NP_000760.1:n.*137A>G
Search 100 bp 5'
Search 100 bp 3'