Canonical Allele Identifier: CA5616768
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs188851578
ExAC: 10:96609674 G / C
gnomAD v2: 10-96609674-G-C
gnomAD v3: 10-94849917-G-C
gnomAD v4: 10-94849917-G-C
MyVariant Identifiers: chr10:g.96609674G>C (hg19) chr10:g.94849917G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849917G>C , CM000672.2:g.94849917G>C GRCh38
NC_000010.10:g.96609674G>C , CM000672.1:g.96609674G>C GRCh37
NC_000010.9:g.96599664G>C NCBI36
NG_008384.2:g.92212G>C
NG_008384.3:g.92237G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150G>C MANE Select ENSP00000360372.3:p.Gly384Arg
ENST00000645461.1:n.2061G>C
ENST00000371321.7:c.1150G>C ENSP00000360372.3:p.Gly384Arg
ENST00000464755.1:c.1913G>C ENSP00000483243.1:n.1913G>C
NM_000769.2:c.1150G>C NP_000760.1:p.Gly384Arg
NM_000769.4:c.1150G>C MANE Select NP_000760.1:p.Gly384Arg
Search 100 bp 5'
Search 100 bp 3'