Canonical Allele Identifier: CA5616431
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs766813172
ExAC: 10:96535225 G / A
gnomAD v2: 10-96535225-G-A
gnomAD v3: 10-94775468-G-A
gnomAD v4: 10-94775468-G-A
MyVariant Identifiers: chr10:g.96535225G>A (hg19) chr10:g.94775468G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775468G>A , CM000672.2:g.94775468G>A GRCh38
NC_000010.10:g.96535225G>A , CM000672.1:g.96535225G>A GRCh37
NC_000010.9:g.96525215G>A NCBI36
NG_008384.2:g.17763G>A
NG_008384.3:g.17788G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.410G>A MANE Select ENSP00000360372.3:p.Gly137Glu
ENST00000645461.1:n.1463G>A
ENST00000371321.7:c.410G>A ENSP00000360372.3:p.Gly137Glu
ENST00000464755.1:c.1173G>A ENSP00000483243.1:n.1173G>A
ENST00000480405.2:c.410G>A ENSP00000483847.1:p.Gly137Glu
NM_000769.2:c.410G>A NP_000760.1:p.Gly137Glu
NM_000769.4:c.410G>A MANE Select NP_000760.1:p.Gly137Glu
Search 100 bp 5'
Search 100 bp 3'