Canonical Allele Identifier: CA3002196681
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-81C>T ENSP00000360372.3:n.-81C>T
ENST00000464755.1:c.932-12433C>T ENSP00000483243.1:n.932-12433C>T