Canonical Allele Identifier: CA2610264767
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781678C>A , CM000672.2:g.94781678C>A GRCh38
NC_000010.10:g.96541435C>A , CM000672.1:g.96541435C>A GRCh37
NC_000010.9:g.96531425C>A NCBI36
NG_008384.2:g.23973C>A
NG_008384.3:g.23998C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-143C>A MANE Select ENSP00000360372.3:n.643-143C>A
ENST00000645461.1:n.1696-143C>A
ENST00000371321.7:c.643-143C>A ENSP00000360372.3:n.643-143C>A
ENST00000464755.1:c.1406-143C>A ENSP00000483243.1:n.1406-143C>A
NM_000769.2:c.643-143C>A NP_000760.1:n.643-143C>A
NM_000769.4:c.643-143C>A MANE Select NP_000760.1:n.643-143C>A