Canonical Allele Identifier: CA5616528
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs753510310
ExAC: 10:96541591 T / A
gnomAD v2: 10-96541591-T-A
gnomAD v4: 10-94781834-T-A
MyVariant Identifiers: chr10:g.96541591T>A (hg19) chr10:g.94781834T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781834T>A , CM000672.2:g.94781834T>A GRCh38
NC_000010.10:g.96541591T>A , CM000672.1:g.96541591T>A GRCh37
NC_000010.9:g.96531581T>A NCBI36
NG_008384.2:g.24129T>A
NG_008384.3:g.24154T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.656T>A MANE Select ENSP00000360372.3:p.Phe219Tyr
ENST00000645461.1:n.1709T>A
ENST00000371321.7:c.656T>A ENSP00000360372.3:p.Phe219Tyr
ENST00000464755.1:c.1419T>A ENSP00000483243.1:n.1419T>A
NM_000769.2:c.656T>A NP_000760.1:p.Phe219Tyr
NM_000769.4:c.656T>A MANE Select NP_000760.1:p.Phe219Tyr
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