Canonical Allele Identifier: CA931378373
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782257_94782260del , CM000672.2:g.94782257_94782260del GRCh38
NC_000010.10:g.96542014_96542017del , CM000672.1:g.96542014_96542017del GRCh37
NC_000010.9:g.96532004_96532007del NCBI36
NG_008384.2:g.24552_24555del
NG_008384.3:g.24577_24580del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+260_819+263del MANE Select ENSP00000360372.3:n.819+260_819+263del
ENST00000645461.1:n.1872+260_1872+263del
ENST00000371321.7:c.819+260_819+263del ENSP00000360372.3:n.819+260_819+263del
ENST00000464755.1:c.1582+260_1582+263del ENSP00000483243.1:n.1582+260_1582+263del
NM_000769.2:c.819+260_819+263del NP_000760.1:n.819+260_819+263del
NM_000769.4:c.819+260_819+263del MANE Select NP_000760.1:n.819+260_819+263del