Canonical Allele Identifier: CA2533034530

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782238G>T , CM000672.2:g.94782238G>T	GRCh38
NC_000010.10:g.96541995G>T , CM000672.1:g.96541995G>T	GRCh37
NC_000010.9:g.96531985G>T	NCBI36
NG_008384.2:g.24533G>T
NG_008384.3:g.24558G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+241G>T MANE Select	ENSP00000360372.3:n.819+241G>T
ENST00000645461.1:n.1872+241G>T
ENST00000371321.7:c.819+241G>T	ENSP00000360372.3:n.819+241G>T
ENST00000464755.1:c.1582+241G>T	ENSP00000483243.1:n.1582+241G>T
NM_000769.2:c.819+241G>T	NP_000760.1:n.819+241G>T
NM_000769.4:c.819+241G>T MANE Select	NP_000760.1:n.819+241G>T