Canonical Allele Identifier: CA377671536
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781992G>C , CM000672.2:g.94781992G>C GRCh38
NC_000010.10:g.96541749G>C , CM000672.1:g.96541749G>C GRCh37
NC_000010.9:g.96531739G>C NCBI36
NG_008384.2:g.24287G>C
NG_008384.3:g.24312G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.814G>C MANE Select ENSP00000360372.3:p.Glu272Gln
ENST00000645461.1:n.1867G>C
ENST00000371321.7:c.814G>C ENSP00000360372.3:p.Glu272Gln
ENST00000464755.1:c.1577G>C ENSP00000483243.1:n.1577G>C
NM_000769.2:c.814G>C NP_000760.1:p.Glu272Gln
NM_000769.4:c.814G>C MANE Select NP_000760.1:p.Glu272Gln