Canonical Allele Identifier: CA913203336
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 633856
ClinVar RCV Id: RCV000782440 RCV000782448 RCV000782449 RCV000782450 RCV000782451 RCV000782452 RCV000782453 RCV000782488 RCV000782513 RCV000782514 RCV000782515 RCV000782516 RCV000782517 RCV000782518 RCV000782519 RCV000782634 RCV000782635 RCV000782636 RCV000782637 RCV000782638 RCV000782639 RCV000782640 RCV000782690 RCV000782691 RCV000782692 RCV000782693 RCV000782694 RCV000782695 RCV000782696 RCV000782697 RCV000782698 RCV000782699 RCV000782700 RCV000782880 RCV000782881 RCV000782882 RCV000782883 RCV000782884 RCV000782885 RCV000782886 RCV000782887 RCV000783140 RCV000783141 RCV000783142 RCV000783143 RCV000783144 RCV000783145 RCV000783171 RCV000783172 RCV000783173 RCV000783174 RCV000783175 RCV000783269 RCV000783270 RCV000783415 RCV000783416 RCV000783417 RCV000783418 RCV000783500 RCV000783514 RCV000783515 RCV000783575 RCV000783576 RCV000783577 RCV000783578 RCV000783613 RCV000783614 RCV000783615 RCV000783616 RCV000783617 RCV000783618 RCV000783619 RCV000783620 RCV000783648 RCV000783666 RCV000783672 RCV000783673 RCV000783712 RCV000783739 RCV000783740 RCV000783741 RCV000783742 RCV000783743 RCV000783864 RCV000783865 RCV000783866 RCV000783867 RCV000783868 RCV000783922 RCV000783923 RCV000783924 RCV000783925 RCV000783926 RCV000783927 RCV000783928 RCV000783929 RCV000783930 RCV000783931 RCV000783932 RCV000784107 RCV000784108 RCV000784109 RCV000784110 RCV000784111 RCV000784112 RCV000784113 RCV000784114 RCV000784115 RCV000784116 RCV000784117 RCV000784118 RCV000784302 RCV000784312 RCV000784313 RCV000784314 RCV000784315 RCV000784316 RCV000784317 RCV000784403 RCV000784404 RCV000784405 RCV000784406 RCV000784407 RCV000784408 RCV000784498 RCV000784499 RCV000784500 RCV000784501 RCV000784502 RCV000784503 RCV000784504 RCV000784505 RCV000784648 RCV000784649 RCV000784650 RCV000784651 RCV000784652 RCV000784653 RCV000784749 RCV000784750 RCV000784751 RCV000784752 RCV000784797 RCV000784798 RCV000784838 RCV000784839 RCV000784840

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.[94775367A>G;94781859G>A] , CM000672.2:g.[94775367A>G;94781859G>A] GRCh38
NC_000010.10:g.[96535124A>G;96541616G>A] , CM000672.1:g.[96535124A>G;96541616G>A] GRCh37
NC_000010.9:g.[96525114A>G;96531606G>A] NCBI36
NG_008384.2:g.[17662A>G;24154G>A]
NG_008384.3:g.[17687A>G;24179G>A]

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.[332-23A>G;681G>A] MANE Select ENSP00000360372.3:p.Pro227=
ENST00000645461.1:n.[1385-23A>G;1734G>A]
ENST00000371321.7:c.[332-23A>G;681G>A] ENSP00000360372.3:p.Pro227=
ENST00000464755.1:c.[1095-23A>G;1444G>A] ENSP00000483243.1:n.[1095-23A>G;1444G>A]
NM_000769.2:c.[332-23A>G;681G>A] NP_000760.1:p.Pro227=
NM_000769.4:c.[332-23A>G;681G>A] MANE Select NP_000760.1:p.Pro227=