Canonical Allele Identifier: CA377671313
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781893T>G , CM000672.2:g.94781893T>G GRCh38
NC_000010.10:g.96541650T>G , CM000672.1:g.96541650T>G GRCh37
NC_000010.9:g.96531640T>G NCBI36
NG_008384.2:g.24188T>G
NG_008384.3:g.24213T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.715T>G MANE Select ENSP00000360372.3:p.Phe239Val
ENST00000645461.1:n.1768T>G
ENST00000371321.7:c.715T>G ENSP00000360372.3:p.Phe239Val
ENST00000464755.1:c.1478T>G ENSP00000483243.1:n.1478T>G
NM_000769.2:c.715T>G NP_000760.1:p.Phe239Val
NM_000769.4:c.715T>G MANE Select NP_000760.1:p.Phe239Val