Canonical Allele Identifier: CA377675774
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1437042029
gnomAD v2: 10-96612507-G-A
gnomAD v4: 10-94852750-G-A
MyVariant Identifiers: chr10:g.96612507G>A (hg19) chr10:g.94852750G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852750G>A , CM000672.2:g.94852750G>A GRCh38
NC_000010.10:g.96612507G>A , CM000672.1:g.96612507G>A GRCh37
NC_000010.9:g.96602497G>A NCBI36
NG_008384.2:g.95045G>A
NG_008384.3:g.95070G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1309G>A MANE Select ENSP00000360372.3:p.Gly437Arg
ENST00000645461.1:n.2220G>A
ENST00000371321.7:c.1309G>A ENSP00000360372.3:p.Gly437Arg
ENST00000464755.1:c.2072G>A ENSP00000483243.1:n.2072G>A
NM_000769.2:c.1309G>A NP_000760.1:p.Gly437Arg
NM_000769.4:c.1309G>A MANE Select NP_000760.1:p.Gly437Arg
Search 100 bp 5'
Search 100 bp 3'