Canonical Allele Identifier: CA377670423
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780504C>G , CM000672.2:g.94780504C>G GRCh38
NC_000010.10:g.96540261C>G , CM000672.1:g.96540261C>G GRCh37
NC_000010.9:g.96530251C>G NCBI36
NG_008384.2:g.22799C>G
NG_008384.3:g.22824C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.487C>G MANE Select ENSP00000360372.3:p.Pro163Ala
ENST00000371321.7:c.487C>G ENSP00000360372.3:p.Pro163Ala
ENST00000464755.1:n.1250C>G ENSP00000483243.1:p.=
NM_000769.2:c.487C>G NP_000760.1:p.Pro163Ala
NM_000769.4:c.487C>G MANE Select NP_000760.1:p.Pro163Ala