Canonical Allele Identifier: CA4369781

Gene: CYP3A4

Linked Data

• dbSNP Id: rs776921395
• ExAC: 7:99367770 G / A
• gnomAD v2: 7-99367770-G-A
• gnomAD v4: 7-99770147-G-A
• MyVariant Identifiers: chr7:g.99367770G>A (hg19) ; chr7:g.99770147G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99770147G>A , CM000669.2:g.99770147G>A	GRCh38
NC_000007.13:g.99367770G>A , CM000669.1:g.99367770G>A	GRCh37
NC_000007.12:g.99205706G>A	NCBI36
NG_008421.1:g.19039C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.407C>T	ENSP00000337915.3:p.Thr136Ile
ENST00000651514.1:c.407C>T MANE Select	ENSP00000498939.1:p.Thr136Ile
ENST00000651783.1:c.58-1640C>T	ENSP00000498924.1:n.58-1640C>T
ENST00000652018.1:c.260C>T	ENSP00000498733.1:p.Thr87Ile
ENST00000336411.6:c.407C>T	ENSP00000337915.2:p.Thr136Ile
ENST00000354593.6:c.72-1645C>T	ENSP00000346607.2:n.72-1645C>T
ENST00000415003.1:c.446C>T	ENSP00000397208.1:p.Thr149Ile
ENST00000480043.1:n.304C>T
NM_001202855.2:c.407C>T	NP_001189784.1:p.Thr136Ile
NM_017460.5:c.407C>T	NP_059488.2:p.Thr136Ile
XM_011515841.1:c.407C>T	XP_011514143.1:p.Thr136Ile
XM_011515842.1:c.407C>T	XP_011514144.1:p.Thr136Ile
NM_017460.6:c.407C>T MANE Select	NP_059488.2:p.Thr136Ile
NM_001202855.3:c.407C>T	NP_001189784.1:p.Thr136Ile