Canonical Allele Identifier: CA456690225

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815581210
• gnomAD v4: 7-99769808-T-G
• MyVariant Identifiers: chr7:g.99367431T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769808T>G , CM000669.2:g.99769808T>G	GRCh38
NC_000007.13:g.99367431T>G , CM000669.1:g.99367431T>G	GRCh37
NC_000007.12:g.99205367T>G	NCBI36
NG_008421.1:g.19378A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.481A>C	ENSP00000337915.3:p.Arg161=
ENST00000651514.1:c.481A>C MANE Select	ENSP00000498939.1:p.Arg161=
ENST00000651783.1:c.58-1301A>C	ENSP00000498924.1:n.58-1301A>C
ENST00000652018.1:c.334A>C	ENSP00000498733.1:p.Arg112=
ENST00000336411.6:c.481A>C	ENSP00000337915.2:p.Arg161=
ENST00000354593.6:c.72-1306A>C	ENSP00000346607.2:n.72-1306A>C
ENST00000480043.1:n.378A>C
NM_001202855.2:c.481A>C	NP_001189784.1:p.Arg161=
NM_017460.5:c.481A>C	NP_059488.2:p.Arg161=
XM_011515841.1:c.481A>C	XP_011514143.1:p.Arg161=
XM_011515842.1:c.481A>C	XP_011514144.1:p.Arg161=
NM_017460.6:c.481A>C MANE Select	NP_059488.2:p.Arg161=
NM_001202855.3:c.481A>C	NP_001189784.1:p.Arg161=