Canonical Allele Identifier: CA5616430
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs374950950
ExAC: 10:96535224 G / C
gnomAD v2: 10-96535224-G-C
gnomAD v4: 10-94775467-G-C
MyVariant Identifiers: chr10:g.96535224G>C (hg19) chr10:g.94775467G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775467G>C , CM000672.2:g.94775467G>C GRCh38
NC_000010.10:g.96535224G>C , CM000672.1:g.96535224G>C GRCh37
NC_000010.9:g.96525214G>C NCBI36
NG_008384.2:g.17762G>C
NG_008384.3:g.17787G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.409G>C MANE Select ENSP00000360372.3:p.Gly137Arg
ENST00000645461.1:n.1462G>C
ENST00000371321.7:c.409G>C ENSP00000360372.3:p.Gly137Arg
ENST00000464755.1:c.1172G>C ENSP00000483243.1:n.1172G>C
ENST00000480405.2:c.409G>C ENSP00000483847.1:p.Gly137Arg
NM_000769.2:c.409G>C NP_000760.1:p.Gly137Arg
NM_000769.4:c.409G>C MANE Select NP_000760.1:p.Gly137Arg
Search 100 bp 5'
Search 100 bp 3'