Canonical Allele Identifier: CA931389759
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849515584
gnomAD v3: 10-94842795-A-G
gnomAD v4: 10-94842795-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94842795A>G , CM000672.2:g.94842795A>G GRCh38
NC_000010.10:g.96602552A>G , CM000672.1:g.96602552A>G GRCh37
NC_000010.9:g.96592542A>G NCBI36
NG_008384.2:g.85090A>G
NG_008384.3:g.85115A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.962-42A>G MANE Select ENSP00000360372.3:n.962-42A>G
ENST00000645461.1:n.1873-42A>G
ENST00000371321.7:c.962-42A>G ENSP00000360372.3:n.962-42A>G
ENST00000464755.1:c.1725-42A>G ENSP00000483243.1:n.1725-42A>G
NM_000769.2:c.962-42A>G NP_000760.1:n.962-42A>G
NM_000769.4:c.962-42A>G MANE Select NP_000760.1:n.962-42A>G
Search 100 bp 5'
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