Canonical Allele Identifier: CA5616314

Gene: CYP2C19

Linked Data

• dbSNP Id: rs769135473
• ExAC: 10:96522637 A / G
• gnomAD v2: 10-96522637-A-G
• gnomAD v3: 10-94762880-A-G
• gnomAD v4: 10-94762880-A-G
• COSMIC: COSM1603878
• MyVariant Identifiers: chr10:g.96522637A>G (hg19) ; chr10:g.94762880A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762880A>G , CM000672.2:g.94762880A>G	GRCh38
NC_000010.10:g.96522637A>G , CM000672.1:g.96522637A>G	GRCh37
NC_000010.9:g.96512627A>G	NCBI36
NG_008384.2:g.5175A>G
NG_008384.3:g.5200A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.168+7A>G MANE Select	ENSP00000360372.3:n.168+7A>G
ENST00000371321.7:c.168+7A>G	ENSP00000360372.3:n.168+7A>G
ENST00000464755.1:c.932-12178A>G	ENSP00000483243.1:n.932-12178A>G
ENST00000480405.2:c.168+7A>G	ENSP00000483847.1:n.168+7A>G
NM_000769.2:c.168+7A>G	NP_000760.1:n.168+7A>G
NM_000769.4:c.168+7A>G MANE Select	NP_000760.1:n.168+7A>G