Canonical Allele Identifier: CA2610262452
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762640-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762640C>G , CM000672.2:g.94762640C>G GRCh38
NC_000010.10:g.96522397C>G , CM000672.1:g.96522397C>G GRCh37
NC_000010.9:g.96512387C>G NCBI36
NG_008384.2:g.4935C>G
NG_008384.3:g.4960C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-66C>G ENSP00000360372.3:n.-66C>G
ENST00000464755.1:c.932-12418C>G ENSP00000483243.1:n.932-12418C>G
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