Canonical Allele Identifier: CA2789069727

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94842804C>T , CM000672.2:g.94842804C>T	GRCh38
NC_000010.10:g.96602561C>T , CM000672.1:g.96602561C>T	GRCh37
NC_000010.9:g.96592551C>T	NCBI36
NG_008384.2:g.85099C>T
NG_008384.3:g.85124C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.962-33C>T MANE Select	ENSP00000360372.3:n.962-33C>T
ENST00000645461.1:n.1873-33C>T
ENST00000371321.7:c.962-33C>T	ENSP00000360372.3:n.962-33C>T
ENST00000464755.1:c.1725-33C>T	ENSP00000483243.1:n.1725-33C>T
NM_000769.2:c.962-33C>T	NP_000760.1:n.962-33C>T
NM_000769.4:c.962-33C>T MANE Select	NP_000760.1:n.962-33C>T