Canonical Allele Identifier: CA1929213627
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762709G= , CM000672.2:g.94762709G= GRCh38
NC_000010.10:g.96522466G= , CM000672.1:g.96522466G= GRCh37
NC_000010.9:g.96512456G= NCBI36
NG_008384.2:g.5004G=
NG_008384.3:g.5029G=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.4G= MANE Select ENSP00000360372.3:p.Asp2=
ENST00000371321.7:c.4G= ENSP00000360372.3:p.Asp2=
ENST00000464755.1:c.932-12349G= ENSP00000483243.1:n.932-12349G=
ENST00000480405.2:c.4G= ENSP00000483847.1:p.Asp2=
NM_000769.2:c.4G= NP_000760.1:p.Asp2=
NM_000769.4:c.4G= MANE Select NP_000760.1:p.Asp2=