Canonical Allele Identifier: CA211697101
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs776343249
gnomAD v4: 10-94852991-G-A
MyVariant Identifiers: chr10:g.96612748G>A (hg19) chr10:g.94852991G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852991G>A , CM000672.2:g.94852991G>A GRCh38
NC_000010.10:g.96612748G>A , CM000672.1:g.96612748G>A GRCh37
NC_000010.9:g.96602738G>A NCBI36
NG_008384.2:g.95286G>A
NG_008384.3:g.95311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*77G>A MANE Select ENSP00000360372.3:n.*77G>A
ENST00000645461.1:n.2461G>A
ENST00000371321.7:c.*77G>A ENSP00000360372.3:n.*77G>A
ENST00000464755.1:c.2313G>A ENSP00000483243.1:n.2313G>A
NM_000769.2:c.*77G>A NP_000760.1:n.*77G>A
NM_000769.4:c.*77G>A MANE Select NP_000760.1:n.*77G>A
Search 100 bp 5'
Search 100 bp 3'