Canonical Allele Identifier: CA377671539
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781993A>G , CM000672.2:g.94781993A>G GRCh38
NC_000010.10:g.96541750A>G , CM000672.1:g.96541750A>G GRCh37
NC_000010.9:g.96531740A>G NCBI36
NG_008384.2:g.24288A>G
NG_008384.3:g.24313A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.815A>G MANE Select ENSP00000360372.3:p.Glu272Gly
ENST00000645461.1:n.1868A>G
ENST00000371321.7:c.815A>G ENSP00000360372.3:p.Glu272Gly
ENST00000464755.1:c.1578A>G ENSP00000483243.1:n.1578A>G
NM_000769.2:c.815A>G NP_000760.1:p.Glu272Gly
NM_000769.4:c.815A>G MANE Select NP_000760.1:p.Glu272Gly