Canonical Allele Identifier: CA470824210
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96522558C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762801C>G , CM000672.2:g.94762801C>G GRCh38
NC_000010.10:g.96522558C>G , CM000672.1:g.96522558C>G GRCh37
NC_000010.9:g.96512548C>G NCBI36
NG_008384.2:g.5096C>G
NG_008384.3:g.5121C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.96C>G MANE Select ENSP00000360372.3:p.Gly32=
ENST00000371321.7:c.96C>G ENSP00000360372.3:p.Gly32=
ENST00000464755.1:c.932-12257C>G ENSP00000483243.1:n.932-12257C>G
ENST00000480405.2:c.96C>G ENSP00000483847.1:p.Gly32=
NM_000769.2:c.96C>G NP_000760.1:p.Gly32=
NM_000769.4:c.96C>G MANE Select NP_000760.1:p.Gly32=
Search 100 bp 5'
Search 100 bp 3'