Canonical Allele Identifier: CA1929213532
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762648G= , CM000672.2:g.94762648G= GRCh38
NC_000010.10:g.96522405G= , CM000672.1:g.96522405G= GRCh37
NC_000010.9:g.96512395G= NCBI36
NG_008384.2:g.4943G=
NG_008384.3:g.4968G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.7:c.-58G= ENSP00000360372.3:n.-58G=
ENST00000464755.1:c.932-12410G= ENSP00000483243.1:n.932-12410G=