Canonical Allele Identifier: CA377670227

Gene: CYP2C19

Linked Data

• COSMIC: COSM3441946
• MyVariant Identifiers: chr10:g.96535251C>T (hg19) ; chr10:g.94775494C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775494C>T , CM000672.2:g.94775494C>T	GRCh38
NC_000010.10:g.96535251C>T , CM000672.1:g.96535251C>T	GRCh37
NC_000010.9:g.96525241C>T	NCBI36
NG_008384.2:g.17789C>T
NG_008384.3:g.17814C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.436C>T MANE Select	ENSP00000360372.3:p.Gln146Ter
ENST00000645461.1:n.1489C>T
ENST00000371321.7:c.436C>T	ENSP00000360372.3:p.Gln146Ter
ENST00000464755.1:c.1199C>T	ENSP00000483243.1:n.1199C>T
ENST00000480405.2:c.436C>T	ENSP00000483847.1:p.Gln146Ter
NM_000769.2:c.436C>T	NP_000760.1:p.Gln146Ter
NM_000769.4:c.436C>T MANE Select	NP_000760.1:p.Gln146Ter