Canonical Allele Identifier: CA1929218662
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775250T= , CM000672.2:g.94775250T= GRCh38
NC_000010.10:g.96535007T= , CM000672.1:g.96535007T= GRCh37
NC_000010.9:g.96524997T= NCBI36
NG_008384.2:g.17545T=
NG_008384.3:g.17570T=

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.331+30T= MANE Select ENSP00000360372.3:n.331+30T=
ENST00000645461.1:n.1384+30T=
ENST00000371321.7:c.331+30T= ENSP00000360372.3:n.331+30T=
ENST00000464755.1:c.1094+30T= ENSP00000483243.1:n.1094+30T=
ENST00000480405.2:c.331+30T= ENSP00000483847.1:n.331+30T=
NM_000769.2:c.331+30T= NP_000760.1:n.331+30T=
NM_000769.4:c.331+30T= MANE Select NP_000760.1:n.331+30T=