Canonical Allele Identifier: CA1929279974
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852943T= , CM000672.2:g.94852943T= GRCh38
NC_000010.10:g.96612700T= , CM000672.1:g.96612700T= GRCh37
NC_000010.9:g.96602690T= NCBI36
NG_008384.2:g.95238T=
NG_008384.3:g.95263T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*29T= MANE Select ENSP00000360372.3:n.*29T=
ENST00000645461.1:n.2413T=
ENST00000371321.7:c.*29T= ENSP00000360372.3:n.*29T=
ENST00000464755.1:c.2265T= ENSP00000483243.1:n.2265T=
NM_000769.2:c.*29T= NP_000760.1:n.*29T=
NM_000769.4:c.*29T= MANE Select NP_000760.1:n.*29T=