Canonical Allele Identifier: CA1929221630
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94780632C= , CM000672.2:g.94780632C= GRCh38
NC_000010.10:g.96540389C= , CM000672.1:g.96540389C= GRCh37
NC_000010.9:g.96530379C= NCBI36
NG_008384.2:g.22927C=
NG_008384.3:g.22952C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.615C= MANE Select ENSP00000360372.3:p.Ile205=
ENST00000645461.1:n.1668C=
ENST00000371321.7:c.615C= ENSP00000360372.3:p.Ile205=
ENST00000464755.1:c.1378C= ENSP00000483243.1:n.1378C=
NM_000769.2:c.615C= NP_000760.1:p.Ile205=
NM_000769.4:c.615C= MANE Select NP_000760.1:p.Ile205=
Search 100 bp 5'
Search 100 bp 3'