Canonical Allele Identifier: CA377670762

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1564662986
• gnomAD v2: 10-96540385-A-T
• gnomAD v4: 10-94780628-A-T
• MyVariant Identifiers: chr10:g.96540385A>T (hg19) ; chr10:g.96540385_96540388delinsTCAT (hg19) ; chr10:g.94780628A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780628A>T , CM000672.2:g.94780628A>T	GRCh38
NC_000010.10:g.96540385A>T , CM000672.1:g.96540385A>T	GRCh37
NC_000010.9:g.96530375A>T	NCBI36
NG_008384.2:g.22923A>T
NG_008384.3:g.22948A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.611A>T MANE Select	ENSP00000360372.3:p.Asn204Ile
ENST00000645461.1:n.1664A>T
ENST00000371321.7:c.611A>T	ENSP00000360372.3:p.Asn204Ile
ENST00000464755.1:c.1374A>T	ENSP00000483243.1:n.1374A>T
NM_000769.2:c.611A>T	NP_000760.1:p.Asn204Ile
NM_000769.4:c.611A>T MANE Select	NP_000760.1:p.Asn204Ile