Canonical Allele Identifier: CA1929279966
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849677919
gnomAD v4: 10-94852928-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852928G>T , CM000672.2:g.94852928G>T GRCh38
NC_000010.10:g.96612685G>T , CM000672.1:g.96612685G>T GRCh37
NC_000010.9:g.96602675G>T NCBI36
NG_008384.2:g.95223G>T
NG_008384.3:g.95248G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*14G>T MANE Select ENSP00000360372.3:n.*14G>T
ENST00000645461.1:n.2398G>T
ENST00000371321.7:c.*14G>T ENSP00000360372.3:n.*14G>T
ENST00000464755.1:c.2250G>T ENSP00000483243.1:n.2250G>T
NM_000769.2:c.*14G>T NP_000760.1:n.*14G>T
NM_000769.4:c.*14G>T MANE Select NP_000760.1:n.*14G>T
Search 100 bp 5'
Search 100 bp 3'