Canonical Allele Identifier: CA211682213
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs760312742
gnomAD v3: 10-94782234-A-G
gnomAD v4: 10-94782234-A-G
MyVariant Identifiers: chr10:g.96541991A>G (hg19) chr10:g.94782234A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94782234A>G , CM000672.2:g.94782234A>G GRCh38
NC_000010.10:g.96541991A>G , CM000672.1:g.96541991A>G GRCh37
NC_000010.9:g.96531981A>G NCBI36
NG_008384.2:g.24529A>G
NG_008384.3:g.24554A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.819+237A>G MANE Select ENSP00000360372.3:n.819+237A>G
ENST00000645461.1:n.1872+237A>G
ENST00000371321.7:c.819+237A>G ENSP00000360372.3:n.819+237A>G
ENST00000464755.1:c.1582+237A>G ENSP00000483243.1:n.1582+237A>G
NM_000769.2:c.819+237A>G NP_000760.1:n.819+237A>G
NM_000769.4:c.819+237A>G MANE Select NP_000760.1:n.819+237A>G
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