Canonical Allele Identifier: CA2610264620
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780698_94780699del , CM000672.2:g.94780698_94780699del GRCh38
NC_000010.10:g.96540455_96540456del , CM000672.1:g.96540455_96540456del GRCh37
NC_000010.9:g.96530445_96530446del NCBI36
NG_008384.2:g.22993_22994del
NG_008384.3:g.23018_23019del

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+39_642+40del MANE Select ENSP00000360372.3:n.642+39_642+40del
ENST00000645461.1:n.1695+39_1695+40del
ENST00000371321.7:c.642+39_642+40del ENSP00000360372.3:n.642+39_642+40del
ENST00000464755.1:c.1405+39_1405+40del ENSP00000483243.1:n.1405+39_1405+40del
NM_000769.2:c.642+39_642+40del NP_000760.1:n.642+39_642+40del
NM_000769.4:c.642+39_642+40del MANE Select NP_000760.1:n.642+39_642+40del