Canonical Allele Identifier: CA377670535
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780558A>T , CM000672.2:g.94780558A>T GRCh38
NC_000010.10:g.96540315A>T , CM000672.1:g.96540315A>T GRCh37
NC_000010.9:g.96530305A>T NCBI36
NG_008384.2:g.22853A>T
NG_008384.3:g.22878A>T

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.541A>T NP_000760.1:p.Ile181Phe
NM_000769.4:c.541A>T MANE Select NP_000760.1:p.Ile181Phe
ENST00000371321.7:c.541A>T ENSP00000360372.3:p.Ile181Phe
ENST00000464755.1:n.1304A>T ENSP00000483243.1:p.=