Canonical Allele Identifier: CA2610265132
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94852583-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852583T>C , CM000672.2:g.94852583T>C GRCh38
NC_000010.10:g.96612340T>C , CM000672.1:g.96612340T>C GRCh37
NC_000010.9:g.96602330T>C NCBI36
NG_008384.2:g.94878T>C
NG_008384.3:g.94903T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1292-150T>C MANE Select ENSP00000360372.3:n.1292-150T>C
ENST00000645461.1:n.2203-150T>C
ENST00000371321.7:c.1292-150T>C ENSP00000360372.3:n.1292-150T>C
ENST00000464755.1:c.2055-150T>C ENSP00000483243.1:n.2055-150T>C
NM_000769.2:c.1292-150T>C NP_000760.1:n.1292-150T>C
NM_000769.4:c.1292-150T>C MANE Select NP_000760.1:n.1292-150T>C
Search 100 bp 5'
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