Canonical Allele Identifier: CA2715605185

Gene: CYP3A4

Linked Data

• dbSNP Id: rs2151559632

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769418C>A , CM000669.2:g.99769418C>A	GRCh38
NC_000007.13:g.99367041C>A , CM000669.1:g.99367041C>A	GRCh37
NC_000007.12:g.99204977C>A	NCBI36
NG_008421.1:g.19768G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+350G>T	ENSP00000337915.3:n.521+350G>T
ENST00000651514.1:c.521+350G>T MANE Select	ENSP00000498939.1:n.521+350G>T
ENST00000651783.1:c.58-911G>T	ENSP00000498924.1:n.58-911G>T
ENST00000652018.1:c.374+350G>T	ENSP00000498733.1:n.374+350G>T
ENST00000336411.6:c.521+350G>T	ENSP00000337915.2:n.521+350G>T
ENST00000354593.6:c.72-916G>T	ENSP00000346607.2:n.72-916G>T
NM_001202855.2:c.521+350G>T	NP_001189784.1:n.521+350G>T
NM_017460.5:c.521+350G>T	NP_059488.2:n.521+350G>T
XM_011515841.1:c.521+350G>T	XP_011514143.1:n.521+350G>T
XM_011515842.1:c.521+350G>T	XP_011514144.1:n.521+350G>T
NM_017460.6:c.521+350G>T MANE Select	NP_059488.2:n.521+350G>T
NM_001202855.3:c.521+350G>T	NP_001189784.1:n.521+350G>T