Canonical Allele Identifier: CA1929222182
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781691A= , CM000672.2:g.94781691A= GRCh38
NC_000010.10:g.96541448A= , CM000672.1:g.96541448A= GRCh37
NC_000010.9:g.96531438A= NCBI36
NG_008384.2:g.23986A=
NG_008384.3:g.24011A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.643-130A= MANE Select ENSP00000360372.3:n.643-130A=
ENST00000645461.1:n.1696-130A=
ENST00000371321.7:c.643-130A= ENSP00000360372.3:n.643-130A=
ENST00000464755.1:c.1406-130A= ENSP00000483243.1:n.1406-130A=
NM_000769.2:c.643-130A= NP_000760.1:n.643-130A=
NM_000769.4:c.643-130A= MANE Select NP_000760.1:n.643-130A=