Canonical Allele Identifier: CA2610265342
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853059-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853059T>A , CM000672.2:g.94853059T>A GRCh38
NC_000010.10:g.96612816T>A , CM000672.1:g.96612816T>A GRCh37
NC_000010.9:g.96602806T>A NCBI36
NG_008384.2:g.95354T>A
NG_008384.3:g.95379T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*145T>A MANE Select ENSP00000360372.3:n.*145T>A
ENST00000645461.1:n.2529T>A
ENST00000371321.7:c.*145T>A ENSP00000360372.3:n.*145T>A
ENST00000464755.1:c.2381T>A ENSP00000483243.1:n.2381T>A
NM_000769.2:c.*145T>A NP_000760.1:n.*145T>A
NM_000769.4:c.*145T>A MANE Select NP_000760.1:n.*145T>A
Search 100 bp 5'
Search 100 bp 3'