Canonical Allele Identifier: CA1929222858
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848487747
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782158A>C , CM000672.2:g.94782158A>C GRCh38
NC_000010.10:g.96541915A>C , CM000672.1:g.96541915A>C GRCh37
NC_000010.9:g.96531905A>C NCBI36
NG_008384.2:g.24453A>C
NG_008384.3:g.24478A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+161A>C MANE Select ENSP00000360372.3:n.819+161A>C
ENST00000645461.1:n.1872+161A>C
ENST00000371321.7:c.819+161A>C ENSP00000360372.3:n.819+161A>C
ENST00000464755.1:c.1582+161A>C ENSP00000483243.1:n.1582+161A>C
NM_000769.2:c.819+161A>C NP_000760.1:n.819+161A>C
NM_000769.4:c.819+161A>C MANE Select NP_000760.1:n.819+161A>C
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