Canonical Allele Identifier: CA1929213554
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762668C= , CM000672.2:g.94762668C= GRCh38
NC_000010.10:g.96522425C= , CM000672.1:g.96522425C= GRCh37
NC_000010.9:g.96512415C= NCBI36
NG_008384.2:g.4963C=
NG_008384.3:g.4988C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.7:c.-38C= ENSP00000360372.3:n.-38C=
ENST00000464755.1:c.932-12390C= ENSP00000483243.1:n.932-12390C=