Canonical Allele Identifier: CA470832027
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96540296C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780539C>A , CM000672.2:g.94780539C>A GRCh38
NC_000010.10:g.96540296C>A , CM000672.1:g.96540296C>A GRCh37
NC_000010.9:g.96530286C>A NCBI36
NG_008384.2:g.22834C>A
NG_008384.3:g.22859C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.522C>A MANE Select ENSP00000360372.3:p.Pro174=
ENST00000645461.1:n.1575C>A
ENST00000371321.7:c.522C>A ENSP00000360372.3:p.Pro174=
ENST00000464755.1:c.1285C>A ENSP00000483243.1:n.1285C>A
NM_000769.2:c.522C>A NP_000760.1:p.Pro174=
NM_000769.4:c.522C>A MANE Select NP_000760.1:p.Pro174=