Canonical Allele Identifier: CA595638631
Gene: CYP2C19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780463T>C , CM000672.2:g.94780463T>C GRCh38
NC_000010.10:g.96540220T>C , CM000672.1:g.96540220T>C GRCh37
NC_000010.9:g.96530210T>C NCBI36
NG_008384.2:g.22758T>C
NG_008384.3:g.22783T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.482-36T>C MANE Select ENSP00000360372.3:p.=
ENST00000371321.7:c.482-36T>C ENSP00000360372.3:p.=
ENST00000464755.1:n.1245-36T>C ENSP00000483243.1:p.=
NM_000769.2:c.482-36T>C NP_000760.1:p.=
NM_000769.4:c.482-36T>C MANE Select NP_000760.1:p.=