Canonical Allele Identifier: CA470832914
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96609754T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849997T>A , CM000672.2:g.94849997T>A GRCh38
NC_000010.10:g.96609754T>A , CM000672.1:g.96609754T>A GRCh37
NC_000010.9:g.96599744T>A NCBI36
NG_008384.2:g.92292T>A
NG_008384.3:g.92317T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1230T>A MANE Select ENSP00000360372.3:p.Arg410=
ENST00000645461.1:n.2141T>A
ENST00000371321.7:c.1230T>A ENSP00000360372.3:p.Arg410=
ENST00000464755.1:c.1993T>A ENSP00000483243.1:n.1993T>A
NM_000769.2:c.1230T>A NP_000760.1:p.Arg410=
NM_000769.4:c.1230T>A MANE Select NP_000760.1:p.Arg410=
Search 100 bp 5'
Search 100 bp 3'