Canonical Allele Identifier: CA2610262451
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762639-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762639G>A , CM000672.2:g.94762639G>A GRCh38
NC_000010.10:g.96522396G>A , CM000672.1:g.96522396G>A GRCh37
NC_000010.9:g.96512386G>A NCBI36
NG_008384.2:g.4934G>A
NG_008384.3:g.4959G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-67G>A ENSP00000360372.3:n.-67G>A
ENST00000464755.1:c.932-12419G>A ENSP00000483243.1:n.932-12419G>A
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