Canonical Allele Identifier: CA377670493

Gene: CYP2C19

Linked Data

• dbSNP Id: rs753980288
• gnomAD v4: 10-94780538-C-T
• COSMIC: COSM3441951
• MyVariant Identifiers: chr10:g.96540295C>T (hg19) ; chr10:g.94780538C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94780538C>T , CM000672.2:g.94780538C>T	GRCh38
NC_000010.10:g.96540295C>T , CM000672.1:g.96540295C>T	GRCh37
NC_000010.9:g.96530285C>T	NCBI36
NG_008384.2:g.22833C>T
NG_008384.3:g.22858C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.521C>T MANE Select	ENSP00000360372.3:p.Pro174Leu
ENST00000645461.1:n.1574C>T
ENST00000371321.7:c.521C>T	ENSP00000360372.3:p.Pro174Leu
ENST00000464755.1:c.1284C>T	ENSP00000483243.1:n.1284C>T
NM_000769.2:c.521C>T	NP_000760.1:p.Pro174Leu
NM_000769.4:c.521C>T MANE Select	NP_000760.1:p.Pro174Leu