Canonical Allele Identifier: CA2574628715
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852942G>T , CM000672.2:g.94852942G>T GRCh38
NC_000010.10:g.96612699G>T , CM000672.1:g.96612699G>T GRCh37
NC_000010.9:g.96602689G>T NCBI36
NG_008384.2:g.95237G>T
NG_008384.3:g.95262G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*28G>T MANE Select ENSP00000360372.3:n.*28G>T
ENST00000645461.1:n.2412G>T
ENST00000371321.7:c.*28G>T ENSP00000360372.3:n.*28G>T
ENST00000464755.1:c.2264G>T ENSP00000483243.1:n.2264G>T
NM_000769.2:c.*28G>T NP_000760.1:n.*28G>T
NM_000769.4:c.*28G>T MANE Select NP_000760.1:n.*28G>T
Search 100 bp 5'
Search 100 bp 3'