Canonical Allele Identifier: CA377669718
Gene: CYP2C19 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.96534932G>C (hg19) chr10:g.94775175G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775175G>C , CM000672.2:g.94775175G>C GRCh38
NC_000010.10:g.96534932G>C , CM000672.1:g.96534932G>C GRCh37
NC_000010.9:g.96524922G>C NCBI36
NG_008384.2:g.17470G>C
NG_008384.3:g.17495G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.286G>C MANE Select ENSP00000360372.3:p.Gly96Arg
ENST00000645461.1:n.1339G>C
ENST00000371321.7:c.286G>C ENSP00000360372.3:p.Gly96Arg
ENST00000464755.1:c.1049G>C ENSP00000483243.1:n.1049G>C
ENST00000480405.2:c.286G>C ENSP00000483847.1:p.Gly96Arg
NM_000769.2:c.286G>C NP_000760.1:p.Gly96Arg
NM_000769.4:c.286G>C MANE Select NP_000760.1:p.Gly96Arg
Search 100 bp 5'
Search 100 bp 3'