Canonical Allele Identifier: CA377675758
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852742T>G , CM000672.2:g.94852742T>G GRCh38
NC_000010.10:g.96612499T>G , CM000672.1:g.96612499T>G GRCh37
NC_000010.9:g.96602489T>G NCBI36
NG_008384.2:g.95037T>G
NG_008384.3:g.95062T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1301T>G MANE Select ENSP00000360372.3:p.Ile434Ser
ENST00000645461.1:n.2212T>G
ENST00000371321.7:c.1301T>G ENSP00000360372.3:p.Ile434Ser
ENST00000464755.1:c.2064T>G ENSP00000483243.1:n.2064T>G
NM_000769.2:c.1301T>G NP_000760.1:p.Ile434Ser
NM_000769.4:c.1301T>G MANE Select NP_000760.1:p.Ile434Ser