Canonical Allele Identifier: CA595324586
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1197325538
gnomAD v2: 10-96612812-T-A
gnomAD v3: 10-94853055-T-A
gnomAD v4: 10-94853055-T-A
MyVariant Identifiers: chr10:g.96612812T>A (hg19) chr10:g.94853055T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853055T>A , CM000672.2:g.94853055T>A GRCh38
NC_000010.10:g.96612812T>A , CM000672.1:g.96612812T>A GRCh37
NC_000010.9:g.96602802T>A NCBI36
NG_008384.2:g.95350T>A
NG_008384.3:g.95375T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*141T>A MANE Select ENSP00000360372.3:n.*141T>A
ENST00000645461.1:n.2525T>A
ENST00000371321.7:c.*141T>A ENSP00000360372.3:n.*141T>A
ENST00000464755.1:c.2377T>A ENSP00000483243.1:n.2377T>A
NM_000769.2:c.*141T>A NP_000760.1:n.*141T>A
NM_000769.4:c.*141T>A MANE Select NP_000760.1:n.*141T>A
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