Canonical Allele Identifier: CA2610262450
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762635-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762635A>T , CM000672.2:g.94762635A>T GRCh38
NC_000010.10:g.96522392A>T , CM000672.1:g.96522392A>T GRCh37
NC_000010.9:g.96512382A>T NCBI36
NG_008384.2:g.4930A>T
NG_008384.3:g.4955A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-71A>T ENSP00000360372.3:n.-71A>T
ENST00000464755.1:c.932-12423A>T ENSP00000483243.1:n.932-12423A>T
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