Canonical Allele Identifier: CA470832037
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540314C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780557C>A , CM000672.2:g.94780557C>A GRCh38
NC_000010.10:g.96540314C>A , CM000672.1:g.96540314C>A GRCh37
NC_000010.9:g.96530304C>A NCBI36
NG_008384.2:g.22852C>A
NG_008384.3:g.22877C>A

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.540C>A NP_000760.1:p.Ser180=
NM_000769.4:c.540C>A MANE Select NP_000760.1:p.Ser180=
ENST00000371321.7:c.540C>A ENSP00000360372.3:p.Ser180=
ENST00000464755.1:n.1303C>A ENSP00000483243.1:p.=