Canonical Allele Identifier: CA2610262453
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762641A>C , CM000672.2:g.94762641A>C GRCh38
NC_000010.10:g.96522398A>C , CM000672.1:g.96522398A>C GRCh37
NC_000010.9:g.96512388A>C NCBI36
NG_008384.2:g.4936A>C
NG_008384.3:g.4961A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-65A>C ENSP00000360372.3:n.-65A>C
ENST00000464755.1:c.932-12417A>C ENSP00000483243.1:n.932-12417A>C