Canonical Allele Identifier: CA470832002
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540260A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780503A>C , CM000672.2:g.94780503A>C GRCh38
NC_000010.10:g.96540260A>C , CM000672.1:g.96540260A>C GRCh37
NC_000010.9:g.96530250A>C NCBI36
NG_008384.2:g.22798A>C
NG_008384.3:g.22823A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.486A>C MANE Select ENSP00000360372.3:p.Ser162=
ENST00000371321.7:c.486A>C ENSP00000360372.3:p.Ser162=
ENST00000464755.1:n.1249A>C ENSP00000483243.1:p.=
NM_000769.2:c.486A>C NP_000760.1:p.Ser162=
NM_000769.4:c.486A>C MANE Select NP_000760.1:p.Ser162=