Canonical Allele Identifier: CA377670479
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780531T>G , CM000672.2:g.94780531T>G GRCh38
NC_000010.10:g.96540288T>G , CM000672.1:g.96540288T>G GRCh37
NC_000010.9:g.96530278T>G NCBI36
NG_008384.2:g.22826T>G
NG_008384.3:g.22851T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.514T>G MANE Select ENSP00000360372.3:p.Cys172Gly
ENST00000645461.1:n.1567T>G
ENST00000371321.7:c.514T>G ENSP00000360372.3:p.Cys172Gly
ENST00000464755.1:c.1277T>G ENSP00000483243.1:n.1277T>G
NM_000769.2:c.514T>G NP_000760.1:p.Cys172Gly
NM_000769.4:c.514T>G MANE Select NP_000760.1:p.Cys172Gly