Canonical Allele Identifier: CA377671180
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1362033140
MyVariant Identifiers: chr10:g.96541614C>G (hg19) chr10:g.94781857C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781857C>G , CM000672.2:g.94781857C>G GRCh38
NC_000010.10:g.96541614C>G , CM000672.1:g.96541614C>G GRCh37
NC_000010.9:g.96531604C>G NCBI36
NG_008384.2:g.24152C>G
NG_008384.3:g.24177C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.679C>G MANE Select ENSP00000360372.3:p.Pro227Ala
ENST00000645461.1:n.1732C>G
ENST00000371321.7:c.679C>G ENSP00000360372.3:p.Pro227Ala
ENST00000464755.1:c.1442C>G ENSP00000483243.1:n.1442C>G
NM_000769.2:c.679C>G NP_000760.1:p.Pro227Ala
NM_000769.4:c.679C>G MANE Select NP_000760.1:p.Pro227Ala
Search 100 bp 5'
Search 100 bp 3'