Canonical Allele Identifier: CA470832004
Gene: CYP2C19 HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.486A>T MANE Select ENSP00000360372.3:p.Ser162=
ENST00000645461.1:n.1539A>T
ENST00000371321.7:c.486A>T ENSP00000360372.3:p.Ser162=
ENST00000464755.1:n.1249A>T ENSP00000483243.1:p.=
NM_000769.2:c.486A>T NP_000760.1:p.Ser162=
NM_000769.4:c.486A>T MANE Select NP_000760.1:p.Ser162=