Canonical Allele Identifier: CA2574628712
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs2134295248
gnomAD v3: 10-94852920-C-T
gnomAD v4: 10-94852920-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94852920C>T , CM000672.2:g.94852920C>T GRCh38
NC_000010.10:g.96612677C>T , CM000672.1:g.96612677C>T GRCh37
NC_000010.9:g.96602667C>T NCBI36
NG_008384.2:g.95215C>T
NG_008384.3:g.95240C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.*6C>T MANE Select ENSP00000360372.3:n.*6C>T
ENST00000645461.1:n.2390C>T
ENST00000371321.7:c.*6C>T ENSP00000360372.3:n.*6C>T
ENST00000464755.1:c.2242C>T ENSP00000483243.1:n.2242C>T
NM_000769.2:c.*6C>T NP_000760.1:n.*6C>T
NM_000769.4:c.*6C>T MANE Select NP_000760.1:n.*6C>T
Search 100 bp 5'
Search 100 bp 3'