Canonical Allele Identifier: CA2610265293
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94853011-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94853011A>T , CM000672.2:g.94853011A>T GRCh38
NC_000010.10:g.96612768A>T , CM000672.1:g.96612768A>T GRCh37
NC_000010.9:g.96602758A>T NCBI36
NG_008384.2:g.95306A>T
NG_008384.3:g.95331A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*97A>T MANE Select ENSP00000360372.3:n.*97A>T
ENST00000645461.1:n.2481A>T
ENST00000371321.7:c.*97A>T ENSP00000360372.3:n.*97A>T
ENST00000464755.1:c.2333A>T ENSP00000483243.1:n.2333A>T
NM_000769.2:c.*97A>T NP_000760.1:n.*97A>T
NM_000769.4:c.*97A>T MANE Select NP_000760.1:n.*97A>T
Search 100 bp 5'
Search 100 bp 3'