Canonical Allele Identifier: CA2610262445
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94762625-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762625C>A , CM000672.2:g.94762625C>A GRCh38
NC_000010.10:g.96522382C>A , CM000672.1:g.96522382C>A GRCh37
NC_000010.9:g.96512372C>A NCBI36
NG_008384.2:g.4920C>A
NG_008384.3:g.4945C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-81C>A ENSP00000360372.3:n.-81C>A
ENST00000464755.1:c.932-12433C>A ENSP00000483243.1:n.932-12433C>A
Search 100 bp 5'
Search 100 bp 3'