Canonical Allele Identifier: CA2610265284
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853003-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853003G>T , CM000672.2:g.94853003G>T GRCh38
NC_000010.10:g.96612760G>T , CM000672.1:g.96612760G>T GRCh37
NC_000010.9:g.96602750G>T NCBI36
NG_008384.2:g.95298G>T
NG_008384.3:g.95323G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*89G>T MANE Select ENSP00000360372.3:n.*89G>T
ENST00000645461.1:n.2473G>T
ENST00000371321.7:c.*89G>T ENSP00000360372.3:n.*89G>T
ENST00000464755.1:c.2325G>T ENSP00000483243.1:n.2325G>T
NM_000769.2:c.*89G>T NP_000760.1:n.*89G>T
NM_000769.4:c.*89G>T MANE Select NP_000760.1:n.*89G>T
Search 100 bp 5'
Search 100 bp 3'