Canonical Allele Identifier: CA211682030
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 39348
ClinVar RCV Id: RCV000782446 RCV000782457 RCV000782553 RCV000782554 RCV000782555 RCV000782556 RCV000782557 RCV000782674 RCV000782675 RCV000782676 RCV000782677 RCV000782678 RCV000782679 RCV000782680 RCV000782681 RCV000782698 RCV000782748 RCV000782749 RCV000782751 RCV000782752 RCV000783020 RCV000783021 RCV000783022 RCV000783023 RCV000783024 RCV000783025 RCV000783026 RCV000783027 RCV000783028 RCV000783029 RCV000783030 RCV000783031 RCV000783098 RCV000783099 RCV000783100 RCV000783101 RCV000783102 RCV000783103 RCV000783163 RCV000783174 RCV000783180 RCV000783190 RCV000783197 RCV000783198 RCV000783199 RCV000783200 RCV000783202 RCV000783339 RCV000783340 RCV000783341 RCV000783486 RCV000783487 RCV000783488 RCV000783489 RCV000783533 RCV000783534 RCV000783535 RCV000783536 RCV000783537 RCV000783595 RCV000783596 RCV000783597 RCV000783598 RCV000783620 RCV000783625 RCV000783634 RCV000783639 RCV000783640 RCV000783641 RCV000783642 RCV000783643 RCV000783658 RCV000783664 RCV000783672 RCV000783679 RCV000783682 RCV000783686 RCV000783689 RCV000783691 RCV000783692 RCV000783721 RCV000783722 RCV000783777 RCV000783778 RCV000783779 RCV000783780 RCV000783781 RCV000783782 RCV000783783 RCV000783908 RCV000783909 RCV000783910 RCV000783911 RCV000783932 RCV000783944 RCV000783945 RCV000783955 RCV000783956 RCV000783963 RCV000783964 RCV000783968 RCV000783969 RCV000783975 RCV000783976 RCV000783977 RCV000783978 RCV000783979 RCV000783980 RCV000783981 RCV000783982 RCV000784254 RCV000784255 RCV000784256 RCV000784257 RCV000784258 RCV000784259 RCV000784260 RCV000784261 RCV000784303 RCV000784396 RCV000784397 RCV000784398 RCV000784399 RCV000784400 RCV000784419 RCV000784426 RCV000784431 RCV000784573 RCV000784574 RCV000784575 RCV000784576 RCV000784577 RCV000784578 RCV000784579 RCV000784721 RCV000784722 RCV000784723 RCV000784724 RCV000784725 RCV000784726 RCV000784740 RCV000784769 RCV000784819 RCV000784820 RCV000784854 RCV000784861 RCV000784867
dbSNP Id: rs72558186
MyVariant Identifiers: chr10:g.96541756T>A (hg19) chr10:g.94781999T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781999T>A , CM000672.2:g.94781999T>A GRCh38
NC_000010.10:g.96541756T>A , CM000672.1:g.96541756T>A GRCh37
NC_000010.9:g.96531746T>A NCBI36
NG_008384.2:g.24294T>A
NG_008384.3:g.24319T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.819+2T>A MANE Select ENSP00000360372.3:n.819+2T>A
ENST00000645461.1:n.1872+2T>A
ENST00000371321.7:c.819+2T>A ENSP00000360372.3:n.819+2T>A
ENST00000464755.1:c.1582+2T>A ENSP00000483243.1:n.1582+2T>A
NM_000769.2:c.819+2T>A NP_000760.1:n.819+2T>A
NM_000769.4:c.819+2T>A MANE Select NP_000760.1:n.819+2T>A
Search 100 bp 5'
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