Canonical Allele Identifier: CA470833149
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852833-A-G
MyVariant Identifiers: chr10:g.96612590A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852833A>G , CM000672.2:g.94852833A>G GRCh38
NC_000010.10:g.96612590A>G , CM000672.1:g.96612590A>G GRCh37
NC_000010.9:g.96602580A>G NCBI36
NG_008384.2:g.95128A>G
NG_008384.3:g.95153A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1392A>G MANE Select ENSP00000360372.3:p.Pro464=
ENST00000645461.1:n.2303A>G
ENST00000371321.7:c.1392A>G ENSP00000360372.3:p.Pro464=
ENST00000464755.1:c.2155A>G ENSP00000483243.1:n.2155A>G
NM_000769.2:c.1392A>G NP_000760.1:p.Pro464=
NM_000769.4:c.1392A>G MANE Select NP_000760.1:p.Pro464=
Search 100 bp 5'
Search 100 bp 3'