Canonical Allele Identifier: CA211696628
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs988912037
gnomAD v3: 10-94852683-C-T
gnomAD v4: 10-94852683-C-T
MyVariant Identifiers: chr10:g.96612440C>T (hg19) chr10:g.94852683C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852683C>T , CM000672.2:g.94852683C>T GRCh38
NC_000010.10:g.96612440C>T , CM000672.1:g.96612440C>T GRCh37
NC_000010.9:g.96602430C>T NCBI36
NG_008384.2:g.94978C>T
NG_008384.3:g.95003C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-50C>T MANE Select ENSP00000360372.3:n.1292-50C>T
ENST00000645461.1:n.2203-50C>T
ENST00000371321.7:c.1292-50C>T ENSP00000360372.3:n.1292-50C>T
ENST00000464755.1:c.2055-50C>T ENSP00000483243.1:n.2055-50C>T
NM_000769.2:c.1292-50C>T NP_000760.1:n.1292-50C>T
NM_000769.4:c.1292-50C>T MANE Select NP_000760.1:n.1292-50C>T
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