Canonical Allele Identifier: CA5616517
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs778044050

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781785A>G , CM000672.2:g.94781785A>G GRCh38
NC_000010.10:g.96541542A>G , CM000672.1:g.96541542A>G GRCh37
NC_000010.9:g.96531532A>G NCBI36
NG_008384.2:g.24080A>G
NG_008384.3:g.24105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.643-36A>G MANE Select ENSP00000360372.3:n.643-36A>G
ENST00000645461.1:n.1696-36A>G
ENST00000371321.7:c.643-36A>G ENSP00000360372.3:n.643-36A>G
ENST00000464755.1:c.1406-36A>G ENSP00000483243.1:n.1406-36A>G
NM_000769.2:c.643-36A>G NP_000760.1:n.643-36A>G
NM_000769.4:c.643-36A>G MANE Select NP_000760.1:n.643-36A>G