Canonical Allele Identifier: CA2574622148
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762664A>G , CM000672.2:g.94762664A>G GRCh38
NC_000010.10:g.96522421A>G , CM000672.1:g.96522421A>G GRCh37
NC_000010.9:g.96512411A>G NCBI36
NG_008384.2:g.4959A>G
NG_008384.3:g.4984A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-42A>G ENSP00000360372.3:n.-42A>G
ENST00000464755.1:c.932-12394A>G ENSP00000483243.1:n.932-12394A>G