Canonical Allele Identifier: CA211697167
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs41317284
MyVariant Identifiers: chr10:g.96612772C>G (hg19) chr10:g.94853015C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853015C>G , CM000672.2:g.94853015C>G GRCh38
NC_000010.10:g.96612772C>G , CM000672.1:g.96612772C>G GRCh37
NC_000010.9:g.96602762C>G NCBI36
NG_008384.2:g.95310C>G
NG_008384.3:g.95335C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*101C>G MANE Select ENSP00000360372.3:n.*101C>G
ENST00000645461.1:n.2485C>G
ENST00000371321.7:c.*101C>G ENSP00000360372.3:n.*101C>G
ENST00000464755.1:c.2337C>G ENSP00000483243.1:n.2337C>G
NM_000769.2:c.*101C>G NP_000760.1:n.*101C>G
NM_000769.4:c.*101C>G MANE Select NP_000760.1:n.*101C>G
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