Canonical Allele Identifier: CA670164133
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1201678239
gnomAD v3: 10-94780367-T-A
gnomAD v4: 10-94780367-T-A
MyVariant Identifiers: chr10:g.96540124T>A (hg19) chr10:g.94780367T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780367T>A , CM000672.2:g.94780367T>A GRCh38
NC_000010.10:g.96540124T>A , CM000672.1:g.96540124T>A GRCh37
NC_000010.9:g.96530114T>A NCBI36
NG_008384.2:g.22662T>A
NG_008384.3:g.22687T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-132T>A MANE Select ENSP00000360372.3:n.482-132T>A
ENST00000645461.1:n.1535-132T>A
ENST00000371321.7:c.482-132T>A ENSP00000360372.3:n.482-132T>A
ENST00000464755.1:c.1245-132T>A ENSP00000483243.1:n.1245-132T>A
NM_000769.2:c.482-132T>A NP_000760.1:n.482-132T>A
NM_000769.4:c.482-132T>A MANE Select NP_000760.1:n.482-132T>A
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