Canonical Allele Identifier: CA377669730

Gene: CYP2C19

Linked Data

• MyVariant Identifiers: chr10:g.96534937A>T (hg19) ; chr10:g.94775180A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775180A>T , CM000672.2:g.94775180A>T	GRCh38
NC_000010.10:g.96534937A>T , CM000672.1:g.96534937A>T	GRCh37
NC_000010.9:g.96524927A>T	NCBI36
NG_008384.2:g.17475A>T
NG_008384.3:g.17500A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.291A>T MANE Select	ENSP00000360372.3:p.Arg97Ser
ENST00000645461.1:n.1344A>T
ENST00000371321.7:c.291A>T	ENSP00000360372.3:p.Arg97Ser
ENST00000464755.1:c.1054A>T	ENSP00000483243.1:n.1054A>T
ENST00000480405.2:c.291A>T	ENSP00000483847.1:p.Arg97Ser
NM_000769.2:c.291A>T	NP_000760.1:p.Arg97Ser
NM_000769.4:c.291A>T MANE Select	NP_000760.1:p.Arg97Ser