Canonical Allele Identifier: CA2610264143
Gene: CYP2C19 HGNC NCBI

Linked Data

gnomAD v4: 10-94775789-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94775789C>A , CM000672.2:g.94775789C>A GRCh38
NC_000010.10:g.96535546C>A , CM000672.1:g.96535546C>A GRCh37
NC_000010.9:g.96525536C>A NCBI36
NG_008384.2:g.18084C>A
NG_008384.3:g.18109C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.481+250C>A MANE Select ENSP00000360372.3:n.481+250C>A
ENST00000645461.1:n.1534+250C>A
ENST00000371321.7:c.481+250C>A ENSP00000360372.3:n.481+250C>A
ENST00000464755.1:c.1244+250C>A ENSP00000483243.1:n.1244+250C>A
ENST00000480405.2:c.*242C>A ENSP00000483847.1:n.*242C>A
NM_000769.2:c.481+250C>A NP_000760.1:n.481+250C>A
NM_000769.4:c.481+250C>A MANE Select NP_000760.1:n.481+250C>A
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