Canonical Allele Identifier: CA1929213553
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1564656857
gnomAD v4: 10-94762664-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762664A>C , CM000672.2:g.94762664A>C GRCh38
NC_000010.10:g.96522421A>C , CM000672.1:g.96522421A>C GRCh37
NC_000010.9:g.96512411A>C NCBI36
NG_008384.2:g.4959A>C
NG_008384.3:g.4984A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-42A>C ENSP00000360372.3:n.-42A>C
ENST00000464755.1:c.932-12394A>C ENSP00000483243.1:n.932-12394A>C
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