Canonical Allele Identifier: CA377671099
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781828A>T , CM000672.2:g.94781828A>T GRCh38
NC_000010.10:g.96541585A>T , CM000672.1:g.96541585A>T GRCh37
NC_000010.9:g.96531575A>T NCBI36
NG_008384.2:g.24123A>T
NG_008384.3:g.24148A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.650A>T MANE Select ENSP00000360372.3:p.Asn217Ile
ENST00000645461.1:n.1703A>T
ENST00000371321.7:c.650A>T ENSP00000360372.3:p.Asn217Ile
ENST00000464755.1:c.1413A>T ENSP00000483243.1:n.1413A>T
NM_000769.2:c.650A>T NP_000760.1:p.Asn217Ile
NM_000769.4:c.650A>T MANE Select NP_000760.1:p.Asn217Ile