Canonical Allele Identifier: CA931367726
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848199083
gnomAD v3: 10-94763352-T-C
gnomAD v4: 10-94763352-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94763352T>C , CM000672.2:g.94763352T>C GRCh38
NC_000010.10:g.96523109T>C , CM000672.1:g.96523109T>C GRCh37
NC_000010.9:g.96513099T>C NCBI36
NG_008384.2:g.5647T>C
NG_008384.3:g.5672T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.168+479T>C MANE Select ENSP00000360372.3:n.168+479T>C
ENST00000371321.7:c.168+479T>C ENSP00000360372.3:n.168+479T>C
ENST00000464755.1:c.932-11706T>C ENSP00000483243.1:n.932-11706T>C
ENST00000480405.2:c.168+479T>C ENSP00000483847.1:n.168+479T>C
NM_000769.2:c.168+479T>C NP_000760.1:n.168+479T>C
NM_000769.4:c.168+479T>C MANE Select NP_000760.1:n.168+479T>C
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