Canonical Allele Identifier: CA2789068219
Gene: CYP2C19 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782292G>A , CM000672.2:g.94782292G>A GRCh38
NC_000010.10:g.96542049G>A , CM000672.1:g.96542049G>A GRCh37
NC_000010.9:g.96532039G>A NCBI36
NG_008384.2:g.24587G>A
NG_008384.3:g.24612G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+295G>A MANE Select ENSP00000360372.3:n.819+295G>A
ENST00000645461.1:n.1872+295G>A
ENST00000371321.7:c.819+295G>A ENSP00000360372.3:n.819+295G>A
ENST00000464755.1:c.1582+295G>A ENSP00000483243.1:n.1582+295G>A
NM_000769.2:c.819+295G>A NP_000760.1:n.819+295G>A
NM_000769.4:c.819+295G>A MANE Select NP_000760.1:n.819+295G>A
Search 100 bp 5'
Search 100 bp 3'