Canonical Allele Identifier: CA377676067

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94852893-G-T
• MyVariant Identifiers: chr10:g.96612650G>T (hg19) ; chr10:g.94852893G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852893G>T , CM000672.2:g.94852893G>T	GRCh38
NC_000010.10:g.96612650G>T , CM000672.1:g.96612650G>T	GRCh37
NC_000010.9:g.96602640G>T	NCBI36
NG_008384.2:g.95188G>T
NG_008384.3:g.95213G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1452G>T MANE Select	ENSP00000360372.3:p.Gln484His
ENST00000645461.1:n.2363G>T
ENST00000371321.7:c.1452G>T	ENSP00000360372.3:p.Gln484His
ENST00000464755.1:c.2215G>T	ENSP00000483243.1:n.2215G>T
NM_000769.2:c.1452G>T	NP_000760.1:p.Gln484His
NM_000769.4:c.1452G>T MANE Select	NP_000760.1:p.Gln484His