Canonical Allele Identifier: CA2610265317
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853033-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853033A>G , CM000672.2:g.94853033A>G GRCh38
NC_000010.10:g.96612790A>G , CM000672.1:g.96612790A>G GRCh37
NC_000010.9:g.96602780A>G NCBI36
NG_008384.2:g.95328A>G
NG_008384.3:g.95353A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*119A>G MANE Select ENSP00000360372.3:n.*119A>G
ENST00000645461.1:n.2503A>G
ENST00000371321.7:c.*119A>G ENSP00000360372.3:n.*119A>G
ENST00000464755.1:c.2355A>G ENSP00000483243.1:n.2355A>G
NM_000769.2:c.*119A>G NP_000760.1:n.*119A>G
NM_000769.4:c.*119A>G MANE Select NP_000760.1:n.*119A>G
Search 100 bp 5'
Search 100 bp 3'