Canonical Allele Identifier: CA1929213999
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1589815192
gnomAD v4: 10-94762906-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762906T>G , CM000672.2:g.94762906T>G GRCh38
NC_000010.10:g.96522663T>G , CM000672.1:g.96522663T>G GRCh37
NC_000010.9:g.96512653T>G NCBI36
NG_008384.2:g.5201T>G
NG_008384.3:g.5226T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.168+33T>G MANE Select ENSP00000360372.3:n.168+33T>G
ENST00000371321.7:c.168+33T>G ENSP00000360372.3:n.168+33T>G
ENST00000464755.1:c.932-12152T>G ENSP00000483243.1:n.932-12152T>G
ENST00000480405.2:c.168+33T>G ENSP00000483847.1:n.168+33T>G
NM_000769.2:c.168+33T>G NP_000760.1:n.168+33T>G
NM_000769.4:c.168+33T>G MANE Select NP_000760.1:n.168+33T>G
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