Canonical Allele Identifier: CA5616270
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs746770214
ExAC: 10:96522434 G / A
gnomAD v2: 10-96522434-G-A
gnomAD v3: 10-94762677-G-A
gnomAD v4: 10-94762677-G-A
MyVariant Identifiers: chr10:g.96522434G>A (hg19) chr10:g.94762677G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762677G>A , CM000672.2:g.94762677G>A GRCh38
NC_000010.10:g.96522434G>A , CM000672.1:g.96522434G>A GRCh37
NC_000010.9:g.96512424G>A NCBI36
NG_008384.2:g.4972G>A
NG_008384.3:g.4997G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-29G>A ENSP00000360372.3:n.-29G>A
ENST00000464755.1:c.932-12381G>A ENSP00000483243.1:n.932-12381G>A
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