Canonical Allele Identifier: CA1929221665
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780692A= , CM000672.2:g.94780692A= GRCh38
NC_000010.10:g.96540449A= , CM000672.1:g.96540449A= GRCh37
NC_000010.9:g.96530439A= NCBI36
NG_008384.2:g.22987A=
NG_008384.3:g.23012A=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+33A= MANE Select ENSP00000360372.3:n.642+33A=
ENST00000645461.1:n.1695+33A=
ENST00000371321.7:c.642+33A= ENSP00000360372.3:n.642+33A=
ENST00000464755.1:c.1405+33A= ENSP00000483243.1:n.1405+33A=
NM_000769.2:c.642+33A= NP_000760.1:n.642+33A=
NM_000769.4:c.642+33A= MANE Select NP_000760.1:n.642+33A=