Canonical Allele Identifier: CA1929280021
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1352142098
gnomAD v4: 10-94853043-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853043G>A , CM000672.2:g.94853043G>A GRCh38
NC_000010.10:g.96612800G>A , CM000672.1:g.96612800G>A GRCh37
NC_000010.9:g.96602790G>A NCBI36
NG_008384.2:g.95338G>A
NG_008384.3:g.95363G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*129G>A MANE Select ENSP00000360372.3:n.*129G>A
ENST00000645461.1:n.2513G>A
ENST00000371321.7:c.*129G>A ENSP00000360372.3:n.*129G>A
ENST00000464755.1:c.2365G>A ENSP00000483243.1:n.2365G>A
NM_000769.2:c.*129G>A NP_000760.1:n.*129G>A
NM_000769.4:c.*129G>A MANE Select NP_000760.1:n.*129G>A
Search 100 bp 5'
Search 100 bp 3'