Canonical Allele Identifier: CA211667020
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs377187278
MyVariant Identifiers: chr10:g.96523122A>G (hg19) chr10:g.94763365A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94763365A>G , CM000672.2:g.94763365A>G GRCh38
NC_000010.10:g.96523122A>G , CM000672.1:g.96523122A>G GRCh37
NC_000010.9:g.96513112A>G NCBI36
NG_008384.2:g.5660A>G
NG_008384.3:g.5685A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.168+492A>G MANE Select ENSP00000360372.3:n.168+492A>G
ENST00000371321.7:c.168+492A>G ENSP00000360372.3:n.168+492A>G
ENST00000464755.1:c.932-11693A>G ENSP00000483243.1:n.932-11693A>G
ENST00000480405.2:c.168+492A>G ENSP00000483847.1:n.168+492A>G
NM_000769.2:c.168+492A>G NP_000760.1:n.168+492A>G
NM_000769.4:c.168+492A>G MANE Select NP_000760.1:n.168+492A>G
Search 100 bp 5'
Search 100 bp 3'