Canonical Allele Identifier: CA2610265345
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853060-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853060T>G , CM000672.2:g.94853060T>G GRCh38
NC_000010.10:g.96612817T>G , CM000672.1:g.96612817T>G GRCh37
NC_000010.9:g.96602807T>G NCBI36
NG_008384.2:g.95355T>G
NG_008384.3:g.95380T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*146T>G MANE Select ENSP00000360372.3:n.*146T>G
ENST00000645461.1:n.2530T>G
ENST00000371321.7:c.*146T>G ENSP00000360372.3:n.*146T>G
ENST00000464755.1:c.2382T>G ENSP00000483243.1:n.2382T>G
NM_000769.2:c.*146T>G NP_000760.1:n.*146T>G
NM_000769.4:c.*146T>G MANE Select NP_000760.1:n.*146T>G
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