Canonical Allele Identifier: CA456690126

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815529966
• MyVariant Identifiers: chr7:g.99366008A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768385A>G , CM000669.2:g.99768385A>G	GRCh38
NC_000007.13:g.99366008A>G , CM000669.1:g.99366008A>G	GRCh37
NC_000007.12:g.99203944A>G	NCBI36
NG_008421.1:g.20801T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.639T>C	ENSP00000337915.3:p.Phe213=
ENST00000651514.1:c.639T>C MANE Select	ENSP00000498939.1:p.Phe213=
ENST00000651783.1:c.180T>C	ENSP00000498924.1:p.Phe60=
ENST00000652018.1:c.492T>C	ENSP00000498733.1:p.Phe164=
ENST00000336411.6:c.639T>C	ENSP00000337915.2:p.Phe213=
ENST00000354593.6:c.189T>C	ENSP00000346607.2:p.Phe63=
NM_001202855.2:c.639T>C	NP_001189784.1:p.Phe213=
NM_017460.5:c.639T>C	NP_059488.2:p.Phe213=
XM_011515841.1:c.639T>C	XP_011514143.1:p.Phe213=
XM_011515842.1:c.639T>C	XP_011514144.1:p.Phe213=
NM_017460.6:c.639T>C MANE Select	NP_059488.2:p.Phe213=
NM_001202855.3:c.639T>C	NP_001189784.1:p.Phe213=