Canonical Allele Identifier: CA1929213555
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848185589
gnomAD v4: 10-94762668-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762668C>A , CM000672.2:g.94762668C>A GRCh38
NC_000010.10:g.96522425C>A , CM000672.1:g.96522425C>A GRCh37
NC_000010.9:g.96512415C>A NCBI36
NG_008384.2:g.4963C>A
NG_008384.3:g.4988C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-38C>A ENSP00000360372.3:n.-38C>A
ENST00000464755.1:c.932-12390C>A ENSP00000483243.1:n.932-12390C>A
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