Canonical Allele Identifier: CA2610264834
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94781825_94781826insAAAA , CM000672.2:g.94781825_94781826insAAAA GRCh38
NC_000010.10:g.96541582_96541583insAAAA , CM000672.1:g.96541582_96541583insAAAA GRCh37
NC_000010.9:g.96531572_96531573insAAAA NCBI36
NG_008384.2:g.24120_24121insAAAA
NG_008384.3:g.24145_24146insAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.647_648insAAAA MANE Select ENSP00000360372.3:p.Cys216Ter
ENST00000645461.1:n.1700_1701insAAAA
ENST00000371321.7:c.647_648insAAAA ENSP00000360372.3:p.Cys216Ter
ENST00000464755.1:c.1410_1411insAAAA ENSP00000483243.1:n.1410_1411insAAAA
NM_000769.2:c.647_648insAAAA NP_000760.1:p.Cys216Ter
NM_000769.4:c.647_648insAAAA MANE Select NP_000760.1:p.Cys216Ter