Canonical Allele Identifier: CA931377391

Gene: CYP2C19

Linked Data

• dbSNP Id: rs17885417
• gnomAD v3: 10-94780223-C-CT
• gnomAD v4: 10-94780223-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780230dup , CM000672.2:g.94780230dup	GRCh38
NC_000010.10:g.96539987dup , CM000672.1:g.96539987dup	GRCh37
NC_000010.9:g.96529977dup	NCBI36
NG_008384.2:g.22525dup
NG_008384.3:g.22550dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.482-269dup MANE Select	ENSP00000360372.3:n.482-269dup
ENST00000645461.1:n.1535-269dup
ENST00000371321.7:c.482-269dup	ENSP00000360372.3:n.482-269dup
ENST00000464755.1:c.1245-269dup	ENSP00000483243.1:n.1245-269dup
NM_000769.2:c.482-269dup	NP_000760.1:n.482-269dup
NM_000769.4:c.482-269dup MANE Select	NP_000760.1:n.482-269dup