Canonical Allele Identifier: CA377671431
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs375781227

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781944G>A , CM000672.2:g.94781944G>A GRCh38
NC_000010.10:g.96541701G>A , CM000672.1:g.96541701G>A GRCh37
NC_000010.9:g.96531691G>A NCBI36
NG_008384.2:g.24239G>A
NG_008384.3:g.24264G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.766G>A MANE Select ENSP00000360372.3:p.Asp256Asn
ENST00000645461.1:n.1819G>A
ENST00000371321.7:c.766G>A ENSP00000360372.3:p.Asp256Asn
ENST00000464755.1:c.1529G>A ENSP00000483243.1:n.1529G>A
NM_000769.2:c.766G>A NP_000760.1:p.Asp256Asn
NM_000769.4:c.766G>A MANE Select NP_000760.1:p.Asp256Asn