Canonical Allele Identifier: CA1929219007
Gene: CYP2C19 HGNC NCBI

Linked Data

dbSNP Id: rs1848400550
gnomAD v4: 10-94775820-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775820G>A , CM000672.2:g.94775820G>A GRCh38
NC_000010.10:g.96535577G>A , CM000672.1:g.96535577G>A GRCh37
NC_000010.9:g.96525567G>A NCBI36
NG_008384.2:g.18115G>A
NG_008384.3:g.18140G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+281G>A MANE Select ENSP00000360372.3:n.481+281G>A
ENST00000645461.1:n.1534+281G>A
ENST00000371321.7:c.481+281G>A ENSP00000360372.3:n.481+281G>A
ENST00000464755.1:c.1244+281G>A ENSP00000483243.1:n.1244+281G>A
ENST00000480405.2:c.*273G>A ENSP00000483847.1:n.*273G>A
NM_000769.2:c.481+281G>A NP_000760.1:n.481+281G>A
NM_000769.4:c.481+281G>A MANE Select NP_000760.1:n.481+281G>A
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