Canonical Allele Identifier: CA5616409
Gene: CYP2C19 HGNC NCBI

Linked Data

ClinVar Variation Id: 39351
ClinVar RCV Id: RCV000394401 RCV000782447 RCV000782458 RCV000782558 RCV000782559 RCV000782560 RCV000782561 RCV000782682 RCV000782683 RCV000782684 RCV000782685 RCV000782686 RCV000782687 RCV000782688 RCV000782699 RCV000782700 RCV000782725 RCV000782733 RCV000782750 RCV000782751 RCV000782752 RCV000782753 RCV000782754 RCV000782755 RCV000782756 RCV000782757 RCV000782758 RCV000783032 RCV000783033 RCV000783034 RCV000783035 RCV000783036 RCV000783037 RCV000783038 RCV000783039 RCV000783040 RCV000783104 RCV000783105 RCV000783164 RCV000783165 RCV000783166 RCV000783167 RCV000783168 RCV000783169 RCV000783175 RCV000783181 RCV000783191 RCV000783201 RCV000783202 RCV000783203 RCV000783204 RCV000783205 RCV000783342 RCV000783343 RCV000783344 RCV000783345 RCV000783346 RCV000783347 RCV000783348 RCV000783349 RCV000783490 RCV000783491 RCV000783492 RCV000783493 RCV000783494 RCV000783495 RCV000783496 RCV000783497 RCV000783599 RCV000783600 RCV000783601 RCV000783602 RCV000783626 RCV000783635 RCV000783638 RCV000783643 RCV000783644 RCV000783645 RCV000783646 RCV000783647 RCV000783659 RCV000783665 RCV000783673 RCV000783680 RCV000783683 RCV000783687 RCV000783690 RCV000783692 RCV000783693 RCV000783723 RCV000783724 RCV000783784 RCV000783785 RCV000783786 RCV000783787 RCV000783788 RCV000783789 RCV000783790 RCV000783791 RCV000783912 RCV000783913 RCV000783914 RCV000783915 RCV000783916 RCV000783946 RCV000783947 RCV000783957 RCV000783965 RCV000783970 RCV000783971 RCV000783974 RCV000783983 RCV000783984 RCV000784262 RCV000784263 RCV000784264 RCV000784265 RCV000784266 RCV000784267 RCV000784268 RCV000784269 RCV000784270 RCV000784271 RCV000784272 RCV000784304 RCV000784335 RCV000784336 RCV000784337 RCV000784338 RCV000784420 RCV000784427 RCV000784432 RCV000784580 RCV000784581 RCV000784727 RCV000784728 RCV000784741 RCV000784770 RCV000784771 RCV000784772 RCV000784773 RCV000784774 RCV000784775 RCV000784821 RCV000784822 RCV000784840 RCV000784855 RCV000784862
dbSNP Id: rs41291556
ExAC: 10:96535173 T / C
gnomAD v2: 10-96535173-T-C
gnomAD v3: 10-94775416-T-C
gnomAD v4: 10-94775416-T-C
MyVariant Identifiers: chr10:g.96535173T>C (hg19) chr10:g.94775416T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775416T>C , CM000672.2:g.94775416T>C GRCh38
NC_000010.10:g.96535173T>C , CM000672.1:g.96535173T>C GRCh37
NC_000010.9:g.96525163T>C NCBI36
NG_008384.2:g.17711T>C
NG_008384.3:g.17736T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.358T>C MANE Select ENSP00000360372.3:p.Trp120Arg
ENST00000645461.1:n.1411T>C
ENST00000371321.7:c.358T>C ENSP00000360372.3:p.Trp120Arg
ENST00000464755.1:c.1121T>C ENSP00000483243.1:n.1121T>C
ENST00000480405.2:c.358T>C ENSP00000483847.1:p.Trp120Arg
NM_000769.2:c.358T>C NP_000760.1:p.Trp120Arg
NM_000769.4:c.358T>C MANE Select NP_000760.1:p.Trp120Arg
Search 100 bp 5'
Search 100 bp 3'