Canonical Allele Identifier: CA2610265337

Gene: CYP2C19

Linked Data

• dbSNP Id: rs2134295378
• gnomAD v4: 10-94853053-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94853053C>T , CM000672.2:g.94853053C>T	GRCh38
NC_000010.10:g.96612810C>T , CM000672.1:g.96612810C>T	GRCh37
NC_000010.9:g.96602800C>T	NCBI36
NG_008384.2:g.95348C>T
NG_008384.3:g.95373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*139C>T MANE Select	ENSP00000360372.3:n.*139C>T
ENST00000645461.1:n.2523C>T
ENST00000371321.7:c.*139C>T	ENSP00000360372.3:n.*139C>T
ENST00000464755.1:c.2375C>T	ENSP00000483243.1:n.2375C>T
NM_000769.2:c.*139C>T	NP_000760.1:n.*139C>T
NM_000769.4:c.*139C>T MANE Select	NP_000760.1:n.*139C>T