Canonical Allele Identifier: CA211682178
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs562491622
gnomAD v2: 10-96541951-A-G
gnomAD v3: 10-94782194-A-G
gnomAD v4: 10-94782194-A-G
MyVariant Identifiers: chr10:g.96541951A>G (hg19) chr10:g.94782194A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782194A>G , CM000672.2:g.94782194A>G GRCh38
NC_000010.10:g.96541951A>G , CM000672.1:g.96541951A>G GRCh37
NC_000010.9:g.96531941A>G NCBI36
NG_008384.2:g.24489A>G
NG_008384.3:g.24514A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+197A>G MANE Select ENSP00000360372.3:n.819+197A>G
ENST00000645461.1:n.1872+197A>G
ENST00000371321.7:c.819+197A>G ENSP00000360372.3:n.819+197A>G
ENST00000464755.1:c.1582+197A>G ENSP00000483243.1:n.1582+197A>G
NM_000769.2:c.819+197A>G NP_000760.1:n.819+197A>G
NM_000769.4:c.819+197A>G MANE Select NP_000760.1:n.819+197A>G
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