Canonical Allele Identifier: CA931393599
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1849625022
gnomAD v3: 10-94849821-T-A
gnomAD v4: 10-94849821-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94849821T>A , CM000672.2:g.94849821T>A GRCh38
NC_000010.10:g.96609578T>A , CM000672.1:g.96609578T>A GRCh37
NC_000010.9:g.96599568T>A NCBI36
NG_008384.2:g.92116T>A
NG_008384.3:g.92141T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.1150-96T>A MANE Select ENSP00000360372.3:n.1150-96T>A
ENST00000645461.1:n.2061-96T>A
ENST00000371321.7:c.1150-96T>A ENSP00000360372.3:n.1150-96T>A
ENST00000464755.1:c.1913-96T>A ENSP00000483243.1:n.1913-96T>A
NM_000769.2:c.1150-96T>A NP_000760.1:n.1150-96T>A
NM_000769.4:c.1150-96T>A MANE Select NP_000760.1:n.1150-96T>A
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