Canonical Allele Identifier: CA2610264902
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94782087-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782087G>A , CM000672.2:g.94782087G>A GRCh38
NC_000010.10:g.96541844G>A , CM000672.1:g.96541844G>A GRCh37
NC_000010.9:g.96531834G>A NCBI36
NG_008384.2:g.24382G>A
NG_008384.3:g.24407G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+90G>A MANE Select ENSP00000360372.3:n.819+90G>A
ENST00000645461.1:n.1872+90G>A
ENST00000371321.7:c.819+90G>A ENSP00000360372.3:n.819+90G>A
ENST00000464755.1:c.1582+90G>A ENSP00000483243.1:n.1582+90G>A
NM_000769.2:c.819+90G>A NP_000760.1:n.819+90G>A
NM_000769.4:c.819+90G>A MANE Select NP_000760.1:n.819+90G>A
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