Canonical Allele Identifier: CA470987513

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1324828665
• gnomAD v2: 10-96535262-C-A
• gnomAD v3: 10-94775505-C-A
• gnomAD v4: 10-94775505-C-A
• MyVariant Identifiers: chr10:g.96535262C>A (hg19) ; chr10:g.94775505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775505C>A , CM000672.2:g.94775505C>A	GRCh38
NC_000010.10:g.96535262C>A , CM000672.1:g.96535262C>A	GRCh37
NC_000010.9:g.96525252C>A	NCBI36
NG_008384.2:g.17800C>A
NG_008384.3:g.17825C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.447C>A MANE Select	ENSP00000360372.3:p.Ala149=
ENST00000645461.1:n.1500C>A
ENST00000371321.7:c.447C>A	ENSP00000360372.3:p.Ala149=
ENST00000464755.1:c.1210C>A	ENSP00000483243.1:n.1210C>A
ENST00000480405.2:c.447C>A	ENSP00000483847.1:p.Ala149=
NM_000769.2:c.447C>A	NP_000760.1:p.Ala149=
NM_000769.4:c.447C>A MANE Select	NP_000760.1:p.Ala149=