Canonical Allele Identifier: CA1929279995
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1181518919
gnomAD v4: 10-94852985-A-G
JSON-LD

Genomic Alleles

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

Transcript Alleles

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