Canonical Allele Identifier: CA377670538
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780559T>G , CM000672.2:g.94780559T>G GRCh38
NC_000010.10:g.96540316T>G , CM000672.1:g.96540316T>G GRCh37
NC_000010.9:g.96530306T>G NCBI36
NG_008384.2:g.22854T>G
NG_008384.3:g.22879T>G

Transcript Alleles

HGVS Amino-acid change
NM_000769.2:c.542T>G NP_000760.1:p.Ile181Ser
NM_000769.4:c.542T>G MANE Select NP_000760.1:p.Ile181Ser
ENST00000371321.7:c.542T>G ENSP00000360372.3:p.Ile181Ser
ENST00000464755.1:n.1305T>G ENSP00000483243.1:p.=