Canonical Allele Identifier: CA470832044
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540323C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780566C>T , CM000672.2:g.94780566C>T GRCh38
NC_000010.10:g.96540323C>T , CM000672.1:g.96540323C>T GRCh37
NC_000010.9:g.96530313C>T NCBI36
NG_008384.2:g.22861C>T
NG_008384.3:g.22886C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.549C>T MANE Select ENSP00000360372.3:p.Phe183=
ENST00000645461.1:n.1602C>T
ENST00000371321.7:c.549C>T ENSP00000360372.3:p.Phe183=
ENST00000464755.1:n.1312C>T ENSP00000483243.1:p.=
NM_000769.2:c.549C>T NP_000760.1:p.Phe183=
NM_000769.4:c.549C>T MANE Select NP_000760.1:p.Phe183=