Canonical Allele Identifier: CA470833122
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs118203759
MyVariant Identifiers: chr10:g.96612542C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852785C>T , CM000672.2:g.94852785C>T GRCh38
NC_000010.10:g.96612542C>T , CM000672.1:g.96612542C>T GRCh37
NC_000010.9:g.96602532C>T NCBI36
NG_008384.2:g.95080C>T
NG_008384.3:g.95105C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1344C>T MANE Select ENSP00000360372.3:p.Phe448=
ENST00000645461.1:n.2255C>T
ENST00000371321.7:c.1344C>T ENSP00000360372.3:p.Phe448=
ENST00000464755.1:c.2107C>T ENSP00000483243.1:n.2107C>T
NM_000769.2:c.1344C>T NP_000760.1:p.Phe448=
NM_000769.4:c.1344C>T MANE Select NP_000760.1:p.Phe448=
Search 100 bp 5'
Search 100 bp 3'