Canonical Allele Identifier: CA377675935
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852830C>G , CM000672.2:g.94852830C>G GRCh38
NC_000010.10:g.96612587C>G , CM000672.1:g.96612587C>G GRCh37
NC_000010.9:g.96602577C>G NCBI36
NG_008384.2:g.95125C>G
NG_008384.3:g.95150C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1389C>G MANE Select ENSP00000360372.3:p.Asp463Glu
ENST00000645461.1:n.2300C>G
ENST00000371321.7:c.1389C>G ENSP00000360372.3:p.Asp463Glu
ENST00000464755.1:c.2152C>G ENSP00000483243.1:n.2152C>G
NM_000769.2:c.1389C>G NP_000760.1:p.Asp463Glu
NM_000769.4:c.1389C>G MANE Select NP_000760.1:p.Asp463Glu