Canonical Allele Identifier: CA470831998
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540257T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780500T>A , CM000672.2:g.94780500T>A GRCh38
NC_000010.10:g.96540257T>A , CM000672.1:g.96540257T>A GRCh37
NC_000010.9:g.96530247T>A NCBI36
NG_008384.2:g.22795T>A
NG_008384.3:g.22820T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.483T>A MANE Select ENSP00000360372.3:p.Ala161=
ENST00000371321.7:c.483T>A ENSP00000360372.3:p.Ala161=
ENST00000464755.1:n.1246T>A ENSP00000483243.1:p.=
NM_000769.2:c.483T>A NP_000760.1:p.Ala161=
NM_000769.4:c.483T>A MANE Select NP_000760.1:p.Ala161=