Canonical Allele Identifier: CA931374588

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1848399963
• gnomAD v3: 10-94775781-C-T
• gnomAD v4: 10-94775781-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775781C>T , CM000672.2:g.94775781C>T	GRCh38
NC_000010.10:g.96535538C>T , CM000672.1:g.96535538C>T	GRCh37
NC_000010.9:g.96525528C>T	NCBI36
NG_008384.2:g.18076C>T
NG_008384.3:g.18101C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+242C>T MANE Select	ENSP00000360372.3:n.481+242C>T
ENST00000645461.1:n.1534+242C>T
ENST00000371321.7:c.481+242C>T	ENSP00000360372.3:n.481+242C>T
ENST00000464755.1:c.1244+242C>T	ENSP00000483243.1:n.1244+242C>T
ENST00000480405.2:c.*234C>T	ENSP00000483847.1:n.*234C>T
NM_000769.2:c.481+242C>T	NP_000760.1:n.481+242C>T
NM_000769.4:c.481+242C>T MANE Select	NP_000760.1:n.481+242C>T