Canonical Allele Identifier: CA377671344

Gene: CYP2C19

Linked Data

• gnomAD v4: 10-94781905-G-T
• MyVariant Identifiers: chr10:g.96541662G>T (hg19) ; chr10:g.94781905G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94781905G>T , CM000672.2:g.94781905G>T	GRCh38
NC_000010.10:g.96541662G>T , CM000672.1:g.96541662G>T	GRCh37
NC_000010.9:g.96531652G>T	NCBI36
NG_008384.2:g.24200G>T
NG_008384.3:g.24225G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.727G>T MANE Select	ENSP00000360372.3:p.Asp243Tyr
ENST00000645461.1:n.1780G>T
ENST00000371321.7:c.727G>T	ENSP00000360372.3:p.Asp243Tyr
ENST00000464755.1:c.1490G>T	ENSP00000483243.1:n.1490G>T
NM_000769.2:c.727G>T	NP_000760.1:p.Asp243Tyr
NM_000769.4:c.727G>T MANE Select	NP_000760.1:p.Asp243Tyr