Canonical Allele Identifier: CA470832201
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96541646T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781889T>G , CM000672.2:g.94781889T>G GRCh38
NC_000010.10:g.96541646T>G , CM000672.1:g.96541646T>G GRCh37
NC_000010.9:g.96531636T>G NCBI36
NG_008384.2:g.24184T>G
NG_008384.3:g.24209T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.711T>G MANE Select ENSP00000360372.3:p.Leu237=
ENST00000645461.1:n.1764T>G
ENST00000371321.7:c.711T>G ENSP00000360372.3:p.Leu237=
ENST00000464755.1:c.1474T>G ENSP00000483243.1:n.1474T>G
NM_000769.2:c.711T>G NP_000760.1:p.Leu237=
NM_000769.4:c.711T>G MANE Select NP_000760.1:p.Leu237=