Canonical Allele Identifier: CA368370604

Gene: CYP3A4

Linked Data

• MyVariant Identifiers: chr7:g.99365979A>C (hg19) ; chr7:g.99768356A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768356A>C , CM000669.2:g.99768356A>C	GRCh38
NC_000007.13:g.99365979A>C , CM000669.1:g.99365979A>C	GRCh37
NC_000007.12:g.99203915A>C	NCBI36
NG_008421.1:g.20830T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.668T>G	ENSP00000337915.3:p.Ile223Arg
ENST00000651514.1:c.668T>G MANE Select	ENSP00000498939.1:p.Ile223Arg
ENST00000651783.1:c.209T>G	ENSP00000498924.1:p.Ile70Arg
ENST00000652018.1:c.521T>G	ENSP00000498733.1:p.Ile174Arg
ENST00000336411.6:c.668T>G	ENSP00000337915.2:p.Ile223Arg
ENST00000354593.6:c.218T>G	ENSP00000346607.2:p.Ile73Arg
NM_001202855.2:c.668T>G	NP_001189784.1:p.Ile223Arg
NM_017460.5:c.668T>G	NP_059488.2:p.Ile223Arg
XM_011515841.1:c.668T>G	XP_011514143.1:p.Ile223Arg
XM_011515842.1:c.668T>G	XP_011514144.1:p.Ile223Arg
NM_017460.6:c.668T>G MANE Select	NP_059488.2:p.Ile223Arg
NM_001202855.3:c.668T>G	NP_001189784.1:p.Ile223Arg