Canonical Allele Identifier: CA377675188
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1376847983
gnomAD v2: 10-96609789-G-A
gnomAD v4: 10-94850032-G-A
MyVariant Identifiers: chr10:g.96609789G>A (hg19) chr10:g.94850032G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94850032G>A , CM000672.2:g.94850032G>A GRCh38
NC_000010.10:g.96609789G>A , CM000672.1:g.96609789G>A GRCh37
NC_000010.9:g.96599779G>A NCBI36
NG_008384.2:g.92327G>A
NG_008384.3:g.92352G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1265G>A MANE Select ENSP00000360372.3:p.Ser422Asn
ENST00000645461.1:n.2176G>A
ENST00000371321.7:c.1265G>A ENSP00000360372.3:p.Ser422Asn
ENST00000464755.1:c.2028G>A ENSP00000483243.1:n.2028G>A
NM_000769.2:c.1265G>A NP_000760.1:p.Ser422Asn
NM_000769.4:c.1265G>A MANE Select NP_000760.1:p.Ser422Asn
Search 100 bp 5'
Search 100 bp 3'