Canonical Allele Identifier: CA1104978583

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815525326
• gnomAD v3: 7-99768259-T-G
• gnomAD v4: 7-99768259-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768259T>G , CM000669.2:g.99768259T>G	GRCh38
NC_000007.13:g.99365882T>G , CM000669.1:g.99365882T>G	GRCh37
NC_000007.12:g.99203818T>G	NCBI36
NG_008421.1:g.20927A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.670+95A>C	ENSP00000337915.3:n.670+95A>C
ENST00000651514.1:c.670+95A>C MANE Select	ENSP00000498939.1:n.670+95A>C
ENST00000651783.1:c.211+95A>C	ENSP00000498924.1:n.211+95A>C
ENST00000652018.1:c.523+95A>C	ENSP00000498733.1:n.523+95A>C
ENST00000336411.6:c.670+95A>C	ENSP00000337915.2:n.670+95A>C
ENST00000354593.6:c.220+95A>C	ENSP00000346607.2:n.220+95A>C
NM_001202855.2:c.670+95A>C	NP_001189784.1:n.670+95A>C
NM_017460.5:c.670+95A>C	NP_059488.2:n.670+95A>C
XM_011515841.1:c.670+95A>C	XP_011514143.1:n.670+95A>C
XM_011515842.1:c.670+95A>C	XP_011514144.1:n.670+95A>C
NM_017460.6:c.670+95A>C MANE Select	NP_059488.2:n.670+95A>C
NM_001202855.3:c.670+95A>C	NP_001189784.1:n.670+95A>C