Canonical Allele Identifier: CA2610265278
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852989-G-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852989G>C , CM000672.2:g.94852989G>C GRCh38
NC_000010.10:g.96612746G>C , CM000672.1:g.96612746G>C GRCh37
NC_000010.9:g.96602736G>C NCBI36
NG_008384.2:g.95284G>C
NG_008384.3:g.95309G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*75G>C MANE Select ENSP00000360372.3:n.*75G>C
ENST00000645461.1:n.2459G>C
ENST00000371321.7:c.*75G>C ENSP00000360372.3:n.*75G>C
ENST00000464755.1:c.2311G>C ENSP00000483243.1:n.2311G>C
NM_000769.2:c.*75G>C NP_000760.1:n.*75G>C
NM_000769.4:c.*75G>C MANE Select NP_000760.1:n.*75G>C
Search 100 bp 5'
Search 100 bp 3'