Canonical Allele Identifier: CA377669717

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96534930C>T (hg19) ; chr10:g.94775173C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775173C>T , CM000672.2:g.94775173C>T	GRCh38
NC_000010.10:g.96534930C>T , CM000672.1:g.96534930C>T	GRCh37
NC_000010.9:g.96524920C>T	NCBI36
NG_008384.2:g.17468C>T
NG_008384.3:g.17493C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.284C>T MANE Select	ENSP00000360372.3:p.Ser95Phe
ENST00000645461.1:n.1337C>T
ENST00000371321.7:c.284C>T	ENSP00000360372.3:p.Ser95Phe
ENST00000464755.1:c.1047C>T	ENSP00000483243.1:n.1047C>T
ENST00000480405.2:c.284C>T	ENSP00000483847.1:p.Ser95Phe
NM_000769.2:c.284C>T	NP_000760.1:p.Ser95Phe
NM_000769.4:c.284C>T MANE Select	NP_000760.1:p.Ser95Phe