Canonical Allele Identifier: CA2610264521
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780423_94780433del , CM000672.2:g.94780423_94780433del GRCh38
NC_000010.10:g.96540180_96540190del , CM000672.1:g.96540180_96540190del GRCh37
NC_000010.9:g.96530170_96530180del NCBI36
NG_008384.2:g.22718_22728del
NG_008384.3:g.22743_22753del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-76_482-66del MANE Select ENSP00000360372.3:n.482-76_482-66del
ENST00000645461.1:n.1535-76_1535-66del
ENST00000371321.7:c.482-76_482-66del ENSP00000360372.3:n.482-76_482-66del
ENST00000464755.1:c.1245-76_1245-66del ENSP00000483243.1:n.1245-76_1245-66del
NM_000769.2:c.482-76_482-66del NP_000760.1:n.482-76_482-66del
NM_000769.4:c.482-76_482-66del MANE Select NP_000760.1:n.482-76_482-66del