Canonical Allele Identifier: CA595638595
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs377056911

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775349G>A , CM000672.2:g.94775349G>A GRCh38
NC_000010.10:g.96535106G>A , CM000672.1:g.96535106G>A GRCh37
NC_000010.9:g.96525096G>A NCBI36
NG_008384.2:g.17644G>A
NG_008384.3:g.17669G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.332-41G>A MANE Select ENSP00000360372.3:n.332-41G>A
ENST00000645461.1:n.1385-41G>A
ENST00000371321.7:c.332-41G>A ENSP00000360372.3:n.332-41G>A
ENST00000464755.1:c.1095-41G>A ENSP00000483243.1:n.1095-41G>A
ENST00000480405.2:c.332-41G>A ENSP00000483847.1:n.332-41G>A
NM_000769.2:c.332-41G>A NP_000760.1:n.332-41G>A
NM_000769.4:c.332-41G>A MANE Select NP_000760.1:n.332-41G>A