Canonical Allele Identifier: CA377670512
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848465756
gnomAD v3: 10-94780547-T-A
gnomAD v4: 10-94780547-T-A
MyVariant Identifiers: chr10:g.96540304T>A (hg19) chr10:g.94780547T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780547T>A , CM000672.2:g.94780547T>A GRCh38
NC_000010.10:g.96540304T>A , CM000672.1:g.96540304T>A GRCh37
NC_000010.9:g.96530294T>A NCBI36
NG_008384.2:g.22842T>A
NG_008384.3:g.22867T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.530T>A MANE Select ENSP00000360372.3:p.Val177Glu
ENST00000645461.1:n.1583T>A
ENST00000371321.7:c.530T>A ENSP00000360372.3:p.Val177Glu
ENST00000464755.1:c.1293T>A ENSP00000483243.1:n.1293T>A
NM_000769.2:c.530T>A NP_000760.1:p.Val177Glu
NM_000769.4:c.530T>A MANE Select NP_000760.1:p.Val177Glu
Search 100 bp 5'
Search 100 bp 3'