Canonical Allele Identifier: CA1929221584
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780533T= , CM000672.2:g.94780533T= GRCh38
NC_000010.10:g.96540290T= , CM000672.1:g.96540290T= GRCh37
NC_000010.9:g.96530280T= NCBI36
NG_008384.2:g.22828T=
NG_008384.3:g.22853T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.516T= MANE Select ENSP00000360372.3:p.Cys172=
ENST00000645461.1:n.1569T=
ENST00000371321.7:c.516T= ENSP00000360372.3:p.Cys172=
ENST00000464755.1:c.1279T= ENSP00000483243.1:n.1279T=
NM_000769.2:c.516T= NP_000760.1:p.Cys172=
NM_000769.4:c.516T= MANE Select NP_000760.1:p.Cys172=