Canonical Allele Identifier: CA377670498
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1312470064

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780541G>C , CM000672.2:g.94780541G>C GRCh38
NC_000010.10:g.96540298G>C , CM000672.1:g.96540298G>C GRCh37
NC_000010.9:g.96530288G>C NCBI36
NG_008384.2:g.22836G>C
NG_008384.3:g.22861G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.524G>C MANE Select ENSP00000360372.3:p.Cys175Ser
ENST00000645461.1:n.1577G>C
ENST00000371321.7:c.524G>C ENSP00000360372.3:p.Cys175Ser
ENST00000464755.1:c.1287G>C ENSP00000483243.1:n.1287G>C
NM_000769.2:c.524G>C NP_000760.1:p.Cys175Ser
NM_000769.4:c.524G>C MANE Select NP_000760.1:p.Cys175Ser