Canonical Allele Identifier: CA4369780

Gene: CYP3A4

Linked Data

• dbSNP Id: rs769063899
• ExAC: 7:99367769 G / T
• gnomAD v2: 7-99367769-G-T
• gnomAD v4: 7-99770146-G-T
• MyVariant Identifiers: chr7:g.99367769G>T (hg19) ; chr7:g.99770146G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770146G>T , CM000669.2:g.99770146G>T	GRCh38
NC_000007.13:g.99367769G>T , CM000669.1:g.99367769G>T	GRCh37
NC_000007.12:g.99205705G>T	NCBI36
NG_008421.1:g.19040C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.408C>A	ENSP00000337915.3:p.Thr136=
ENST00000651514.1:c.408C>A MANE Select	ENSP00000498939.1:p.Thr136=
ENST00000651783.1:c.58-1639C>A	ENSP00000498924.1:n.58-1639C>A
ENST00000652018.1:c.261C>A	ENSP00000498733.1:p.Thr87=
ENST00000336411.6:c.408C>A	ENSP00000337915.2:p.Thr136=
ENST00000354593.6:c.72-1644C>A	ENSP00000346607.2:n.72-1644C>A
ENST00000415003.1:c.447C>A	ENSP00000397208.1:p.Thr149=
ENST00000480043.1:n.305C>A
NM_001202855.2:c.408C>A	NP_001189784.1:p.Thr136=
NM_017460.5:c.408C>A	NP_059488.2:p.Thr136=
XM_011515841.1:c.408C>A	XP_011514143.1:p.Thr136=
XM_011515842.1:c.408C>A	XP_011514144.1:p.Thr136=
NM_017460.6:c.408C>A MANE Select	NP_059488.2:p.Thr136=
NM_001202855.3:c.408C>A	NP_001189784.1:p.Thr136=