Canonical Allele Identifier: CA368370606

Gene: CYP3A4

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.668T>C	ENSP00000337915.3:p.Ile223Thr
ENST00000651514.1:c.668T>C MANE Select	ENSP00000498939.1:p.Ile223Thr
ENST00000651783.1:c.209T>C	ENSP00000498924.1:p.Ile70Thr
ENST00000652018.1:c.521T>C	ENSP00000498733.1:p.Ile174Thr
ENST00000336411.6:c.668T>C	ENSP00000337915.2:p.Ile223Thr
ENST00000354593.6:c.218T>C	ENSP00000346607.2:p.Ile73Thr
NM_001202855.2:c.668T>C	NP_001189784.1:p.Ile223Thr
NM_017460.5:c.668T>C	NP_059488.2:p.Ile223Thr
XM_011515841.1:c.668T>C	XP_011514143.1:p.Ile223Thr
XM_011515842.1:c.668T>C	XP_011514144.1:p.Ile223Thr
NM_017460.6:c.668T>C MANE Select	NP_059488.2:p.Ile223Thr
NM_001202855.3:c.668T>C	NP_001189784.1:p.Ile223Thr