Canonical Allele Identifier: CA377671269
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781881A>T , CM000672.2:g.94781881A>T GRCh38
NC_000010.10:g.96541638A>T , CM000672.1:g.96541638A>T GRCh37
NC_000010.9:g.96531628A>T NCBI36
NG_008384.2:g.24176A>T
NG_008384.3:g.24201A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.703A>T MANE Select ENSP00000360372.3:p.Lys235Ter
ENST00000645461.1:n.1756A>T
ENST00000371321.7:c.703A>T ENSP00000360372.3:p.Lys235Ter
ENST00000464755.1:c.1466A>T ENSP00000483243.1:n.1466A>T
NM_000769.2:c.703A>T NP_000760.1:p.Lys235Ter
NM_000769.4:c.703A>T MANE Select NP_000760.1:p.Lys235Ter