Canonical Allele Identifier: CA931395014

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1849669688
• gnomAD v3: 10-94852562-A-T
• gnomAD v4: 10-94852562-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852562A>T , CM000672.2:g.94852562A>T	GRCh38
NC_000010.10:g.96612319A>T , CM000672.1:g.96612319A>T	GRCh37
NC_000010.9:g.96602309A>T	NCBI36
NG_008384.2:g.94857A>T
NG_008384.3:g.94882A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-171A>T MANE Select	ENSP00000360372.3:n.1292-171A>T
ENST00000645461.1:n.2203-171A>T
ENST00000371321.7:c.1292-171A>T	ENSP00000360372.3:n.1292-171A>T
ENST00000464755.1:c.2055-171A>T	ENSP00000483243.1:n.2055-171A>T
NM_000769.2:c.1292-171A>T	NP_000760.1:n.1292-171A>T
NM_000769.4:c.1292-171A>T MANE Select	NP_000760.1:n.1292-171A>T