Canonical Allele Identifier: CA670191450

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1036765817
• gnomAD v3: 10-94762645-A-G
• gnomAD v4: 10-94762645-A-G
• MyVariant Identifiers: chr10:g.96522402A>G (hg19) ; chr10:g.94762645A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762645A>G , CM000672.2:g.94762645A>G	GRCh38
NC_000010.10:g.96522402A>G , CM000672.1:g.96522402A>G	GRCh37
NC_000010.9:g.96512392A>G	NCBI36
NG_008384.2:g.4940A>G
NG_008384.3:g.4965A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.7:c.-61A>G	ENSP00000360372.3:n.-61A>G
ENST00000464755.1:c.932-12413A>G	ENSP00000483243.1:n.932-12413A>G