Canonical Allele Identifier: CA1929221652
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780670G= , CM000672.2:g.94780670G= GRCh38
NC_000010.10:g.96540427G= , CM000672.1:g.96540427G= GRCh37
NC_000010.9:g.96530417G= NCBI36
NG_008384.2:g.22965G=
NG_008384.3:g.22990G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+11G= MANE Select ENSP00000360372.3:n.642+11G=
ENST00000645461.1:n.1695+11G=
ENST00000371321.7:c.642+11G= ENSP00000360372.3:n.642+11G=
ENST00000464755.1:c.1405+11G= ENSP00000483243.1:n.1405+11G=
NM_000769.2:c.642+11G= NP_000760.1:n.642+11G=
NM_000769.4:c.642+11G= MANE Select NP_000760.1:n.642+11G=