Canonical Allele Identifier: CA1929222562
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848485270

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781943_94781944insATAGTGGGAAAATTATTGCATATCTAA , CM000672.2:g.94781943_94781944insATAGTGGGAAAATTATTGCATATCTAA GRCh38
NC_000010.10:g.96541700_96541701insATAGTGGGAAAATTATTGCATATCTAA , CM000672.1:g.96541700_96541701insATAGTGGGAAAATTATTGCATATCTAA GRCh37
NC_000010.9:g.96531690_96531691insATAGTGGGAAAATTATTGCATATCTAA NCBI36
NG_008384.2:g.24238_24239insATAGTGGGAAAATTATTGCATATCTAA
NG_008384.3:g.24263_24264insATAGTGGGAAAATTATTGCATATCTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.765_766insATAGTGGGAAAATTATTGCATATCTAA
ENST00000645461.1:n.1818_1819insATAGTGGGAAAATTATTGCATATCTAA
ENST00000371321.7:c.765_766insATAGTGGGAAAATTATTGCATATCTAA
ENST00000464755.1:c.1528_1529insATAGTGGGAAAATTATTGCATATCTAA ENSP00000483243.1:n.1528_1529insATAGTGGGAAAATTATTGCATATCTAA
NM_000769.2:c.765_766insATAGTGGGAAAATTATTGCATATCTAA
NM_000769.4:c.765_766insATAGTGGGAAAATTATTGCATATCTAA