Canonical Allele Identifier: CA5616470

Gene: CYP2C19

Linked Data

• dbSNP Id: rs776181631
• ExAC: 10:96540250 A / G
• gnomAD v2: 10-96540250-A-G
• gnomAD v3: 10-94780493-A-G
• gnomAD v4: 10-94780493-A-G
• MyVariant Identifiers: chr10:g.96540250A>G (hg19) ; chr10:g.94780493A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780493A>G , CM000672.2:g.94780493A>G	GRCh38
NC_000010.10:g.96540250A>G , CM000672.1:g.96540250A>G	GRCh37
NC_000010.9:g.96530240A>G	NCBI36
NG_008384.2:g.22788A>G
NG_008384.3:g.22813A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.482-6A>G MANE Select	ENSP00000360372.3:n.482-6A>G
ENST00000645461.1:n.1535-6A>G
ENST00000371321.7:c.482-6A>G	ENSP00000360372.3:n.482-6A>G
ENST00000464755.1:c.1245-6A>G	ENSP00000483243.1:n.1245-6A>G
NM_000769.2:c.482-6A>G	NP_000760.1:n.482-6A>G
NM_000769.4:c.482-6A>G MANE Select	NP_000760.1:n.482-6A>G