Canonical Allele Identifier: CA377669602

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1564660997
• MyVariant Identifiers: chr10:g.96534878C>T (hg19) ; chr10:g.94775121C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775121C>T , CM000672.2:g.94775121C>T	GRCh38
NC_000010.10:g.96534878C>T , CM000672.1:g.96534878C>T	GRCh37
NC_000010.9:g.96524868C>T	NCBI36
NG_008384.2:g.17416C>T
NG_008384.3:g.17441C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.232C>T MANE Select	ENSP00000360372.3:p.His78Tyr
ENST00000645461.1:n.1285C>T
ENST00000371321.7:c.232C>T	ENSP00000360372.3:p.His78Tyr
ENST00000464755.1:c.995C>T	ENSP00000483243.1:p.Ala332Val
ENST00000480405.2:c.232C>T	ENSP00000483847.1:p.His78Tyr
NM_000769.2:c.232C>T	NP_000760.1:p.His78Tyr
NM_000769.4:c.232C>T MANE Select	NP_000760.1:p.His78Tyr