Canonical Allele Identifier: CA377675790
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96612514G>C (hg19) chr10:g.94852757G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852757G>C , CM000672.2:g.94852757G>C GRCh38
NC_000010.10:g.96612514G>C , CM000672.1:g.96612514G>C GRCh37
NC_000010.9:g.96602504G>C NCBI36
NG_008384.2:g.95052G>C
NG_008384.3:g.95077G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.1316G>C MANE Select ENSP00000360372.3:p.Gly439Ala
ENST00000645461.1:n.2227G>C
ENST00000371321.7:c.1316G>C ENSP00000360372.3:p.Gly439Ala
ENST00000464755.1:c.2079G>C ENSP00000483243.1:n.2079G>C
NM_000769.2:c.1316G>C NP_000760.1:p.Gly439Ala
NM_000769.4:c.1316G>C MANE Select NP_000760.1:p.Gly439Ala
Search 100 bp 5'
Search 100 bp 3'