Canonical Allele Identifier: CA2789070147
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853045del , CM000672.2:g.94853045del GRCh38
NC_000010.10:g.96612802del , CM000672.1:g.96612802del GRCh37
NC_000010.9:g.96602792del NCBI36
NG_008384.2:g.95340del
NG_008384.3:g.95365del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*131del MANE Select ENSP00000360372.3:n.*131del
ENST00000645461.1:n.2515del
ENST00000371321.7:c.*131del ENSP00000360372.3:n.*131del
ENST00000464755.1:c.2367del ENSP00000483243.1:n.2367del
NM_000769.2:c.*131del NP_000760.1:n.*131del
NM_000769.4:c.*131del MANE Select NP_000760.1:n.*131del