Canonical Allele Identifier: CA470829439

Gene: CYP2C19 MTND4P19

Linked Data

• dbSNP Id: rs1383498810
• gnomAD v4: 10-94774461-A-G
• MyVariant Identifiers: chr10:g.96534218A>G (hg19) ; chr10:g.94774461A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94774461A>G , CM000672.2:g.94774461A>G	GRCh38
NC_000010.10:g.96534218A>G , CM000672.1:g.96534218A>G	GRCh37
NC_000010.9:g.96524208A>G	NCBI36
NG_008384.2:g.16756A>G
NG_008384.3:g.16781A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.169-597A>G (CYP2C19) MANE Select	ENSP00000360372.3:n.169-597A>G
ENST00000645461.1:n.625A>G (CYP2C19)
ENST00000371321.7:c.169-597A>G (CYP2C19)	ENSP00000360372.3:n.169-597A>G
ENST00000446659.1:n.173T>C (MTND4P19)
ENST00000464755.1:c.932-597A>G	ENSP00000483243.1:n.932-597A>G
ENST00000480405.2:c.169-597A>G (CYP2C19)	ENSP00000483847.1:n.169-597A>G
NM_000769.2:c.169-597A>G (CYP2C19)	NP_000760.1:n.169-597A>G
NM_000769.4:c.169-597A>G (CYP2C19) MANE Select	NP_000760.1:n.169-597A>G