Canonical Allele Identifier: CA2610262565
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762805_94762806insGGAGGGAGTT , CM000672.2:g.94762805_94762806insGGAGGGAGTT GRCh38
NC_000010.10:g.96522562_96522563insGGAGGGAGTT , CM000672.1:g.96522562_96522563insGGAGGGAGTT GRCh37
NC_000010.9:g.96512552_96512553insGGAGGGAGTT NCBI36
NG_008384.2:g.5100_5101insGGAGGGAGTT
NG_008384.3:g.5125_5126insGGAGGGAGTT

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.100_101insGGAGGGAGTT MANE Select ENSP00000360372.3:p.Thr34ArgfsTer18
ENST00000371321.7:c.100_101insGGAGGGAGTT ENSP00000360372.3:p.Thr34ArgfsTer18
ENST00000464755.1:c.932-12253_932-12252insGGAGGGAGTT ENSP00000483243.1:n.932-12253_932-12252in...
ENST00000480405.2:c.100_101insGGAGGGAGTT ENSP00000483847.1:p.Thr34ArgfsTer18
NM_000769.2:c.100_101insGGAGGGAGTT NP_000760.1:p.Thr34ArgfsTer18
NM_000769.4:c.100_101insGGAGGGAGTT MANE Select NP_000760.1:p.Thr34ArgfsTer18