Canonical Allele Identifier: CA377671200
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781863A>G , CM000672.2:g.94781863A>G GRCh38
NC_000010.10:g.96541620A>G , CM000672.1:g.96541620A>G GRCh37
NC_000010.9:g.96531610A>G NCBI36
NG_008384.2:g.24158A>G
NG_008384.3:g.24183A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.685A>G MANE Select ENSP00000360372.3:p.Thr229Ala
ENST00000645461.1:n.1738A>G
ENST00000371321.7:c.685A>G ENSP00000360372.3:p.Thr229Ala
ENST00000464755.1:c.1448A>G ENSP00000483243.1:n.1448A>G
NM_000769.2:c.685A>G NP_000760.1:p.Thr229Ala
NM_000769.4:c.685A>G MANE Select NP_000760.1:p.Thr229Ala