Canonical Allele Identifier: CA1929222969
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782264T= , CM000672.2:g.94782264T= GRCh38
NC_000010.10:g.96542021T= , CM000672.1:g.96542021T= GRCh37
NC_000010.9:g.96532011T= NCBI36
NG_008384.2:g.24559T=
NG_008384.3:g.24584T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+267T= MANE Select ENSP00000360372.3:n.819+267T=
ENST00000645461.1:n.1872+267T=
ENST00000371321.7:c.819+267T= ENSP00000360372.3:n.819+267T=
ENST00000464755.1:c.1582+267T= ENSP00000483243.1:n.1582+267T=
NM_000769.2:c.819+267T= NP_000760.1:n.819+267T=
NM_000769.4:c.819+267T= MANE Select NP_000760.1:n.819+267T=
Search 100 bp 5'
Search 100 bp 3'