Canonical Allele Identifier: CA670194231

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1167614505
• MyVariant Identifiers: chr10:g.96610007G>A (hg19) ; chr10:g.94850250G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94850250G>A , CM000672.2:g.94850250G>A	GRCh38
NC_000010.10:g.96610007G>A , CM000672.1:g.96610007G>A	GRCh37
NC_000010.9:g.96599997G>A	NCBI36
NG_008384.2:g.92545G>A
NG_008384.3:g.92570G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1291+192G>A MANE Select	ENSP00000360372.3:n.1291+192G>A
ENST00000645461.1:n.2202+192G>A
ENST00000371321.7:c.1291+192G>A	ENSP00000360372.3:n.1291+192G>A
ENST00000464755.1:c.2054+192G>A	ENSP00000483243.1:n.2054+192G>A
NM_000769.2:c.1291+192G>A	NP_000760.1:n.1291+192G>A
NM_000769.4:c.1291+192G>A MANE Select	NP_000760.1:n.1291+192G>A