Canonical Allele Identifier: CA377669628
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775132A>T , CM000672.2:g.94775132A>T GRCh38
NC_000010.10:g.96534889A>T , CM000672.1:g.96534889A>T GRCh37
NC_000010.9:g.96524879A>T NCBI36
NG_008384.2:g.17427A>T
NG_008384.3:g.17452A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.243A>T MANE Select ENSP00000360372.3:p.Glu81Asp
ENST00000645461.1:n.1296A>T
ENST00000371321.7:c.243A>T ENSP00000360372.3:p.Glu81Asp
ENST00000464755.1:c.1006A>T ENSP00000483243.1:n.1006A>T
ENST00000480405.2:c.243A>T ENSP00000483847.1:p.Glu81Asp
NM_000769.2:c.243A>T NP_000760.1:p.Glu81Asp
NM_000769.4:c.243A>T MANE Select NP_000760.1:p.Glu81Asp