Canonical Allele Identifier: CA211682254
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1005460546
gnomAD v3: 10-94782252-G-GA
gnomAD v4: 10-94782252-G-GA
MyVariant Identifiers: chr10:g.96542009_96542010insA (hg19) chr10:g.94782252_94782253insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782256dup , CM000672.2:g.94782256dup GRCh38
NC_000010.10:g.96542013dup , CM000672.1:g.96542013dup GRCh37
NC_000010.9:g.96532003dup NCBI36
NG_008384.2:g.24551dup
NG_008384.3:g.24576dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+259dup MANE Select ENSP00000360372.3:n.819+259dup
ENST00000645461.1:n.1872+259dup
ENST00000371321.7:c.819+259dup ENSP00000360372.3:n.819+259dup
ENST00000464755.1:c.1582+259dup ENSP00000483243.1:n.1582+259dup
NM_000769.2:c.819+259dup NP_000760.1:n.819+259dup
NM_000769.4:c.819+259dup MANE Select NP_000760.1:n.819+259dup
Search 100 bp 5'
Search 100 bp 3'