Canonical Allele Identifier: CA470832024
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540293T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780536T>A , CM000672.2:g.94780536T>A GRCh38
NC_000010.10:g.96540293T>A , CM000672.1:g.96540293T>A GRCh37
NC_000010.9:g.96530283T>A NCBI36
NG_008384.2:g.22831T>A
NG_008384.3:g.22856T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.519T>A MANE Select ENSP00000360372.3:p.Ala173=
ENST00000645461.1:n.1572T>A
ENST00000371321.7:c.519T>A ENSP00000360372.3:p.Ala173=
ENST00000464755.1:c.1282T>A ENSP00000483243.1:n.1282T>A
NM_000769.2:c.519T>A NP_000760.1:p.Ala173=
NM_000769.4:c.519T>A MANE Select NP_000760.1:p.Ala173=