Canonical Allele Identifier: CA377674996

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94849942-C-T
• MyVariant Identifiers: chr10:g.96609699C>T (hg19) ; chr10:g.94849942C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94849942C>T , CM000672.2:g.94849942C>T	GRCh38
NC_000010.10:g.96609699C>T , CM000672.1:g.96609699C>T	GRCh37
NC_000010.9:g.96599689C>T	NCBI36
NG_008384.2:g.92237C>T
NG_008384.3:g.92262C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1175C>T MANE Select	ENSP00000360372.3:p.Thr392Ile
ENST00000645461.1:n.2086C>T
ENST00000371321.7:c.1175C>T	ENSP00000360372.3:p.Thr392Ile
ENST00000464755.1:c.1938C>T	ENSP00000483243.1:n.1938C>T
NM_000769.2:c.1175C>T	NP_000760.1:p.Thr392Ile
NM_000769.4:c.1175C>T MANE Select	NP_000760.1:p.Thr392Ile