Canonical Allele Identifier: CA470832042
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540320T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780563T>A , CM000672.2:g.94780563T>A GRCh38
NC_000010.10:g.96540320T>A , CM000672.1:g.96540320T>A GRCh37
NC_000010.9:g.96530310T>A NCBI36
NG_008384.2:g.22858T>A
NG_008384.3:g.22883T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.546T>A MANE Select ENSP00000360372.3:p.Ile182=
ENST00000645461.1:n.1599T>A
ENST00000371321.7:c.546T>A ENSP00000360372.3:p.Ile182=
ENST00000464755.1:n.1309T>A ENSP00000483243.1:p.=
NM_000769.2:c.546T>A NP_000760.1:p.Ile182=
NM_000769.4:c.546T>A MANE Select NP_000760.1:p.Ile182=