Canonical Allele Identifier: CA4369864

Gene: CYP3A4

Linked Data

• dbSNP Id: rs779398469
• ExAC: 7:99375704 C / T
• gnomAD v2: 7-99375704-C-T
• gnomAD v4: 7-99778081-C-T
• MyVariant Identifiers: chr7:g.99375704C>T (hg19) ; chr7:g.99778081C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99778081C>T , CM000669.2:g.99778081C>T	GRCh38
NC_000007.13:g.99375704C>T , CM000669.1:g.99375704C>T	GRCh37
NC_000007.12:g.99213640C>T	NCBI36
NG_008421.1:g.11105G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.166-1G>A	ENSP00000337915.3:n.166-1G>A
ENST00000651514.1:c.166-1G>A MANE Select	ENSP00000498939.1:n.166-1G>A
ENST00000651783.1:c.57+5266G>A	ENSP00000498924.1:n.57+5266G>A
ENST00000652018.1:c.72-5392G>A	ENSP00000498733.1:n.72-5392G>A
ENST00000336411.6:c.166-1G>A	ENSP00000337915.2:n.166-1G>A
ENST00000354593.6:c.71+5930G>A	ENSP00000346607.2:n.71+5930G>A
ENST00000415003.1:c.205-1G>A	ENSP00000397208.1:n.205-1G>A
ENST00000480043.1:n.63-1G>A
NM_001202855.2:c.166-1G>A	NP_001189784.1:n.166-1G>A
NM_017460.5:c.166-1G>A	NP_059488.2:n.166-1G>A
XM_011515841.1:c.166-1G>A	XP_011514143.1:n.166-1G>A
XM_011515842.1:c.166-1G>A	XP_011514144.1:n.166-1G>A
NM_017460.6:c.166-1G>A MANE Select	NP_059488.2:n.166-1G>A
NM_001202855.3:c.166-1G>A	NP_001189784.1:n.166-1G>A