Canonical Allele Identifier: CA2789070144

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94853013C>T , CM000672.2:g.94853013C>T	GRCh38
NC_000010.10:g.96612770C>T , CM000672.1:g.96612770C>T	GRCh37
NC_000010.9:g.96602760C>T	NCBI36
NG_008384.2:g.95308C>T
NG_008384.3:g.95333C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*99C>T MANE Select	ENSP00000360372.3:n.*99C>T
ENST00000645461.1:n.2483C>T
ENST00000371321.7:c.*99C>T	ENSP00000360372.3:n.*99C>T
ENST00000464755.1:c.2335C>T	ENSP00000483243.1:n.2335C>T
NM_000769.2:c.*99C>T	NP_000760.1:n.*99C>T
NM_000769.4:c.*99C>T MANE Select	NP_000760.1:n.*99C>T