Canonical Allele Identifier: CA377671273
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781882A>G , CM000672.2:g.94781882A>G GRCh38
NC_000010.10:g.96541639A>G , CM000672.1:g.96541639A>G GRCh37
NC_000010.9:g.96531629A>G NCBI36
NG_008384.2:g.24177A>G
NG_008384.3:g.24202A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.704A>G MANE Select ENSP00000360372.3:p.Lys235Arg
ENST00000645461.1:n.1757A>G
ENST00000371321.7:c.704A>G ENSP00000360372.3:p.Lys235Arg
ENST00000464755.1:c.1467A>G ENSP00000483243.1:n.1467A>G
NM_000769.2:c.704A>G NP_000760.1:p.Lys235Arg
NM_000769.4:c.704A>G MANE Select NP_000760.1:p.Lys235Arg