Canonical Allele Identifier: CA2610265316

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94853031-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94853031C>T , CM000672.2:g.94853031C>T	GRCh38
NC_000010.10:g.96612788C>T , CM000672.1:g.96612788C>T	GRCh37
NC_000010.9:g.96602778C>T	NCBI36
NG_008384.2:g.95326C>T
NG_008384.3:g.95351C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*117C>T MANE Select	ENSP00000360372.3:n.*117C>T
ENST00000645461.1:n.2501C>T
ENST00000371321.7:c.*117C>T	ENSP00000360372.3:n.*117C>T
ENST00000464755.1:c.2353C>T	ENSP00000483243.1:n.2353C>T
NM_000769.2:c.*117C>T	NP_000760.1:n.*117C>T
NM_000769.4:c.*117C>T MANE Select	NP_000760.1:n.*117C>T