Canonical Allele Identifier: CA595638676

Gene: CYP2C19

Linked Data

• dbSNP Id: rs1367316574
• gnomAD v2: 10-96602550-C-T
• gnomAD v3: 10-94842793-C-T
• gnomAD v4: 10-94842793-C-T
• MyVariant Identifiers: chr10:g.96602550C>T (hg19) ; chr10:g.94842793C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94842793C>T , CM000672.2:g.94842793C>T	GRCh38
NC_000010.10:g.96602550C>T , CM000672.1:g.96602550C>T	GRCh37
NC_000010.9:g.96592540C>T	NCBI36
NG_008384.2:g.85088C>T
NG_008384.3:g.85113C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.962-44C>T MANE Select	ENSP00000360372.3:n.962-44C>T
ENST00000645461.1:n.1873-44C>T
ENST00000371321.7:c.962-44C>T	ENSP00000360372.3:n.962-44C>T
ENST00000464755.1:c.1725-44C>T	ENSP00000483243.1:n.1725-44C>T
NM_000769.2:c.962-44C>T	NP_000760.1:n.962-44C>T
NM_000769.4:c.962-44C>T MANE Select	NP_000760.1:n.962-44C>T