Canonical Allele Identifier: CA670196713
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1181518919
gnomAD v4: 10-94852985-A-C
MyVariant Identifiers: chr10:g.96612742A>C (hg19) chr10:g.94852985A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852985A>C , CM000672.2:g.94852985A>C GRCh38
NC_000010.10:g.96612742A>C , CM000672.1:g.96612742A>C GRCh37
NC_000010.9:g.96602732A>C NCBI36
NG_008384.2:g.95280A>C
NG_008384.3:g.95305A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*71A>C MANE Select ENSP00000360372.3:n.*71A>C
ENST00000645461.1:n.2455A>C
ENST00000371321.7:c.*71A>C ENSP00000360372.3:n.*71A>C
ENST00000464755.1:c.2307A>C ENSP00000483243.1:n.2307A>C
NM_000769.2:c.*71A>C NP_000760.1:n.*71A>C
NM_000769.4:c.*71A>C MANE Select NP_000760.1:n.*71A>C
Search 100 bp 5'
Search 100 bp 3'