Canonical Allele Identifier: CA470832036
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540311C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780554C>T , CM000672.2:g.94780554C>T GRCh38
NC_000010.10:g.96540311C>T , CM000672.1:g.96540311C>T GRCh37
NC_000010.9:g.96530301C>T NCBI36
NG_008384.2:g.22849C>T
NG_008384.3:g.22874C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.537C>T MANE Select ENSP00000360372.3:p.Cys179=
ENST00000645461.1:n.1590C>T
ENST00000371321.7:c.537C>T ENSP00000360372.3:p.Cys179=
ENST00000464755.1:n.1300C>T ENSP00000483243.1:p.=
NM_000769.2:c.537C>T NP_000760.1:p.Cys179=
NM_000769.4:c.537C>T MANE Select NP_000760.1:p.Cys179=