Canonical Allele Identifier: CA1104978966

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815568769
• gnomAD v3: 7-99769373-C-G
• gnomAD v4: 7-99769373-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769373C>G , CM000669.2:g.99769373C>G	GRCh38
NC_000007.13:g.99366996C>G , CM000669.1:g.99366996C>G	GRCh37
NC_000007.12:g.99204932C>G	NCBI36
NG_008421.1:g.19813G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+395G>C	ENSP00000337915.3:n.521+395G>C
ENST00000651514.1:c.521+395G>C MANE Select	ENSP00000498939.1:n.521+395G>C
ENST00000651783.1:c.58-866G>C	ENSP00000498924.1:n.58-866G>C
ENST00000652018.1:c.374+395G>C	ENSP00000498733.1:n.374+395G>C
ENST00000336411.6:c.521+395G>C	ENSP00000337915.2:n.521+395G>C
ENST00000354593.6:c.72-871G>C	ENSP00000346607.2:n.72-871G>C
NM_001202855.2:c.521+395G>C	NP_001189784.1:n.521+395G>C
NM_017460.5:c.521+395G>C	NP_059488.2:n.521+395G>C
XM_011515841.1:c.521+395G>C	XP_011514143.1:n.521+395G>C
XM_011515842.1:c.521+395G>C	XP_011514144.1:n.521+395G>C
NM_017460.6:c.521+395G>C MANE Select	NP_059488.2:n.521+395G>C
NM_001202855.3:c.521+395G>C	NP_001189784.1:n.521+395G>C