Canonical Allele Identifier: CA1929213482
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1589815022

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762624A>G , CM000672.2:g.94762624A>G GRCh38
NC_000010.10:g.96522381A>G , CM000672.1:g.96522381A>G GRCh37
NC_000010.9:g.96512371A>G NCBI36
NG_008384.2:g.4919A>G
NG_008384.3:g.4944A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-82A>G ENSP00000360372.3:n.-82A>G
ENST00000464755.1:c.932-12434A>G ENSP00000483243.1:n.932-12434A>G