Canonical Allele Identifier: CA5616297
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs776992052

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762782G>C , CM000672.2:g.94762782G>C GRCh38
NC_000010.10:g.96522539G>C , CM000672.1:g.96522539G>C GRCh37
NC_000010.9:g.96512529G>C NCBI36
NG_008384.2:g.5077G>C
NG_008384.3:g.5102G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.77G>C MANE Select ENSP00000360372.3:p.Arg26Thr
ENST00000371321.7:c.77G>C ENSP00000360372.3:p.Arg26Thr
ENST00000464755.1:c.932-12276G>C ENSP00000483243.1:n.932-12276G>C
ENST00000480405.2:c.77G>C ENSP00000483847.1:p.Arg26Thr
NM_000769.2:c.77G>C NP_000760.1:p.Arg26Thr
NM_000769.4:c.77G>C MANE Select NP_000760.1:p.Arg26Thr