Canonical Allele Identifier: CA377675125
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850005T>A , CM000672.2:g.94850005T>A GRCh38
NC_000010.10:g.96609762T>A , CM000672.1:g.96609762T>A GRCh37
NC_000010.9:g.96599752T>A NCBI36
NG_008384.2:g.92300T>A
NG_008384.3:g.92325T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1238T>A MANE Select ENSP00000360372.3:p.Leu413Gln
ENST00000645461.1:n.2149T>A
ENST00000371321.7:c.1238T>A ENSP00000360372.3:p.Leu413Gln
ENST00000464755.1:c.2001T>A ENSP00000483243.1:n.2001T>A
NM_000769.2:c.1238T>A NP_000760.1:p.Leu413Gln
NM_000769.4:c.1238T>A MANE Select NP_000760.1:p.Leu413Gln