Canonical Allele Identifier: CA5616535
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs770126483

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781871C>T , CM000672.2:g.94781871C>T GRCh38
NC_000010.10:g.96541628C>T , CM000672.1:g.96541628C>T GRCh37
NC_000010.9:g.96531618C>T NCBI36
NG_008384.2:g.24166C>T
NG_008384.3:g.24191C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.693C>T MANE Select ENSP00000360372.3:p.Asn231=
ENST00000645461.1:n.1746C>T
ENST00000371321.7:c.693C>T ENSP00000360372.3:p.Asn231=
ENST00000464755.1:c.1456C>T ENSP00000483243.1:n.1456C>T
NM_000769.2:c.693C>T NP_000760.1:p.Asn231=
NM_000769.4:c.693C>T MANE Select NP_000760.1:p.Asn231=