Canonical Allele Identifier: CA595638708
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs770428716
gnomAD v2: 10-96612444-C-G
gnomAD v4: 10-94852687-C-G
MyVariant Identifiers: chr10:g.96612444C>G (hg19) chr10:g.94852687C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852687C>G , CM000672.2:g.94852687C>G GRCh38
NC_000010.10:g.96612444C>G , CM000672.1:g.96612444C>G GRCh37
NC_000010.9:g.96602434C>G NCBI36
NG_008384.2:g.94982C>G
NG_008384.3:g.95007C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1292-46C>G MANE Select ENSP00000360372.3:n.1292-46C>G
ENST00000645461.1:n.2203-46C>G
ENST00000371321.7:c.1292-46C>G ENSP00000360372.3:n.1292-46C>G
ENST00000464755.1:c.2055-46C>G ENSP00000483243.1:n.2055-46C>G
NM_000769.2:c.1292-46C>G NP_000760.1:n.1292-46C>G
NM_000769.4:c.1292-46C>G MANE Select NP_000760.1:n.1292-46C>G
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