Canonical Allele Identifier: CA377670618

Gene: CYP2C19

Linked Data

• COSMIC: COSM1702801
• MyVariant Identifiers: chr10:g.96540348C>T (hg19) ; chr10:g.94780591C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780591C>T , CM000672.2:g.94780591C>T	GRCh38
NC_000010.10:g.96540348C>T , CM000672.1:g.96540348C>T	GRCh37
NC_000010.9:g.96530338C>T	NCBI36
NG_008384.2:g.22886C>T
NG_008384.3:g.22911C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.574C>T MANE Select	ENSP00000360372.3:p.Gln192Ter
ENST00000645461.1:n.1627C>T
ENST00000371321.7:c.574C>T	ENSP00000360372.3:p.Gln192Ter
ENST00000464755.1:c.1337C>T	ENSP00000483243.1:n.1337C>T
NM_000769.2:c.574C>T	NP_000760.1:p.Gln192Ter
NM_000769.4:c.574C>T MANE Select	NP_000760.1:p.Gln192Ter