Canonical Allele Identifier: CA2610265215
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852680-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852680A>C , CM000672.2:g.94852680A>C GRCh38
NC_000010.10:g.96612437A>C , CM000672.1:g.96612437A>C GRCh37
NC_000010.9:g.96602427A>C NCBI36
NG_008384.2:g.94975A>C
NG_008384.3:g.95000A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-53A>C MANE Select ENSP00000360372.3:n.1292-53A>C
ENST00000645461.1:n.2203-53A>C
ENST00000371321.7:c.1292-53A>C ENSP00000360372.3:n.1292-53A>C
ENST00000464755.1:c.2055-53A>C ENSP00000483243.1:n.2055-53A>C
NM_000769.2:c.1292-53A>C NP_000760.1:n.1292-53A>C
NM_000769.4:c.1292-53A>C MANE Select NP_000760.1:n.1292-53A>C
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