Canonical Allele Identifier: CA913508332
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1564686282
gnomAD v2: 10-96609611-C-A
gnomAD v4: 10-94849854-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849854C>A , CM000672.2:g.94849854C>A GRCh38
NC_000010.10:g.96609611C>A , CM000672.1:g.96609611C>A GRCh37
NC_000010.9:g.96599601C>A NCBI36
NG_008384.2:g.92149C>A
NG_008384.3:g.92174C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-63C>A MANE Select ENSP00000360372.3:n.1150-63C>A
ENST00000645461.1:n.2061-63C>A
ENST00000371321.7:c.1150-63C>A ENSP00000360372.3:n.1150-63C>A
ENST00000464755.1:c.1913-63C>A ENSP00000483243.1:n.1913-63C>A
NM_000769.2:c.1150-63C>A NP_000760.1:n.1150-63C>A
NM_000769.4:c.1150-63C>A MANE Select NP_000760.1:n.1150-63C>A
Search 100 bp 5'
Search 100 bp 3'