Canonical Allele Identifier: CA2574628682
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852685C>A , CM000672.2:g.94852685C>A GRCh38
NC_000010.10:g.96612442C>A , CM000672.1:g.96612442C>A GRCh37
NC_000010.9:g.96602432C>A NCBI36
NG_008384.2:g.94980C>A
NG_008384.3:g.95005C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-48C>A MANE Select ENSP00000360372.3:n.1292-48C>A
ENST00000645461.1:n.2203-48C>A
ENST00000371321.7:c.1292-48C>A ENSP00000360372.3:n.1292-48C>A
ENST00000464755.1:c.2055-48C>A ENSP00000483243.1:n.2055-48C>A
NM_000769.2:c.1292-48C>A NP_000760.1:n.1292-48C>A
NM_000769.4:c.1292-48C>A MANE Select NP_000760.1:n.1292-48C>A
Search 100 bp 5'
Search 100 bp 3'