Canonical Allele Identifier: CA595638628
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1564662897

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780457C>G , CM000672.2:g.94780457C>G GRCh38
NC_000010.10:g.96540214C>G , CM000672.1:g.96540214C>G GRCh37
NC_000010.9:g.96530204C>G NCBI36
NG_008384.2:g.22752C>G
NG_008384.3:g.22777C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-42C>G MANE Select ENSP00000360372.3:n.482-42C>G
ENST00000645461.1:n.1535-42C>G
ENST00000371321.7:c.482-42C>G ENSP00000360372.3:n.482-42C>G
ENST00000464755.1:c.1245-42C>G ENSP00000483243.1:n.1245-42C>G
NM_000769.2:c.482-42C>G NP_000760.1:n.482-42C>G
NM_000769.4:c.482-42C>G MANE Select NP_000760.1:n.482-42C>G