Canonical Allele Identifier: CA2610264619
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780696_94780697insTT , CM000672.2:g.94780696_94780697insTT GRCh38
NC_000010.10:g.96540453_96540454insTT , CM000672.1:g.96540453_96540454insTT GRCh37
NC_000010.9:g.96530443_96530444insTT NCBI36
NG_008384.2:g.22991_22992insTT
NG_008384.3:g.23016_23017insTT

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.642+37_642+38insTT MANE Select ENSP00000360372.3:n.642+37_642+38insTT
ENST00000645461.1:n.1695+37_1695+38insTT
ENST00000371321.7:c.642+37_642+38insTT ENSP00000360372.3:n.642+37_642+38insTT
ENST00000464755.1:c.1405+37_1405+38insTT ENSP00000483243.1:n.1405+37_1405+38insTT
NM_000769.2:c.642+37_642+38insTT NP_000760.1:n.642+37_642+38insTT
NM_000769.4:c.642+37_642+38insTT MANE Select NP_000760.1:n.642+37_642+38insTT