Canonical Allele Identifier: CA1929221627
Gene: CYP2C19 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780628_94780631delinsACAT , CM000672.2:g.94780628_94780631delinsACAT GRCh38
NC_000010.10:g.96540385_96540388delinsACAT , CM000672.1:g.96540385_96540388delinsACAT GRCh37
NC_000010.9:g.96530375_96530378delinsACAT NCBI36
NG_008384.2:g.22923_22926delinsACAT
NG_008384.3:g.22948_22951delinsACAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.611_614delinsACAT MANE Select ENSP00000360372.3:p.Asn204=
ENST00000645461.1:n.1664_1667delinsACAT
ENST00000371321.7:c.611_614delinsACAT ENSP00000360372.3:p.Asn204=
ENST00000464755.1:c.1374_1377delinsACAT ENSP00000483243.1:n.1374_1377delinsACAT
NM_000769.2:c.611_614delinsACAT NP_000760.1:p.Asn204=
NM_000769.4:c.611_614delinsACAT MANE Select NP_000760.1:p.Asn204=
Search 100 bp 5'
Search 100 bp 3'