Canonical Allele Identifier: CA2610262447
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762629-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762629C>A , CM000672.2:g.94762629C>A GRCh38
NC_000010.10:g.96522386C>A , CM000672.1:g.96522386C>A GRCh37
NC_000010.9:g.96512376C>A NCBI36
NG_008384.2:g.4924C>A
NG_008384.3:g.4949C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-77C>A ENSP00000360372.3:n.-77C>A
ENST00000464755.1:c.932-12429C>A ENSP00000483243.1:n.932-12429C>A
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