Canonical Allele Identifier: CA470829740

Gene: CYP2C19 MTND4P19

Linked Data

• dbSNP Id: rs1221399185
• gnomAD v3: 10-94774507-G-A
• gnomAD v4: 10-94774507-G-A
• MyVariant Identifiers: chr10:g.96534264G>A (hg19) ; chr10:g.94774507G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94774507G>A , CM000672.2:g.94774507G>A	GRCh38
NC_000010.10:g.96534264G>A , CM000672.1:g.96534264G>A	GRCh37
NC_000010.9:g.96524254G>A	NCBI36
NG_008384.2:g.16802G>A
NG_008384.3:g.16827G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371321.9:c.169-551G>A (CYP2C19) MANE Select	ENSP00000360372.3:n.169-551G>A
ENST00000645461.1:n.671G>A (CYP2C19)
ENST00000371321.7:c.169-551G>A (CYP2C19)	ENSP00000360372.3:n.169-551G>A
ENST00000446659.1:n.127C>T (MTND4P19)
ENST00000464755.1:c.932-551G>A	ENSP00000483243.1:n.932-551G>A
ENST00000480405.2:c.169-551G>A (CYP2C19)	ENSP00000483847.1:n.169-551G>A
NM_000769.2:c.169-551G>A (CYP2C19)	NP_000760.1:n.169-551G>A
NM_000769.4:c.169-551G>A (CYP2C19) MANE Select	NP_000760.1:n.169-551G>A