Canonical Allele Identifier: CA377667953
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848189072
gnomAD v3: 10-94762769-C-G
gnomAD v4: 10-94762769-C-G
MyVariant Identifiers: chr10:g.96522526C>G (hg19) chr10:g.94762769C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762769C>G , CM000672.2:g.94762769C>G GRCh38
NC_000010.10:g.96522526C>G , CM000672.1:g.96522526C>G GRCh37
NC_000010.9:g.96512516C>G NCBI36
NG_008384.2:g.5064C>G
NG_008384.3:g.5089C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.64C>G MANE Select ENSP00000360372.3:p.Gln22Glu
ENST00000371321.7:c.64C>G ENSP00000360372.3:p.Gln22Glu
ENST00000464755.1:c.932-12289C>G ENSP00000483243.1:n.932-12289C>G
ENST00000480405.2:c.64C>G ENSP00000483847.1:p.Gln22Glu
NM_000769.2:c.64C>G NP_000760.1:p.Gln22Glu
NM_000769.4:c.64C>G MANE Select NP_000760.1:p.Gln22Glu
Search 100 bp 5'
Search 100 bp 3'