Canonical Allele Identifier: CA456686462

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1459636078
• gnomAD v3: 7-99760861-T-C
• gnomAD v4: 7-99760861-T-C
• MyVariant Identifiers: chr7:g.99358484T>C (hg19) ; chr7:g.99760861T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760861T>C , CM000669.2:g.99760861T>C	GRCh38
NC_000007.13:g.99358484T>C , CM000669.1:g.99358484T>C	GRCh37
NC_000007.12:g.99196420T>C	NCBI36
NG_008421.1:g.28325A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1467A>G	ENSP00000337915.3:p.Arg489=
ENST00000651162.1:n.809A>G
ENST00000651514.1:c.1374A>G MANE Select	ENSP00000498939.1:p.Arg458=
ENST00000651783.1:c.915A>G	ENSP00000498924.1:p.Arg305=
ENST00000652018.1:c.1227A>G	ENSP00000498733.1:p.Arg409=
ENST00000336411.6:c.1374A>G	ENSP00000337915.2:p.Arg458=
ENST00000354593.6:c.924A>G	ENSP00000346607.2:p.Arg308=
NM_001202855.2:c.1371A>G	NP_001189784.1:p.Arg457=
NM_017460.5:c.1374A>G	NP_059488.2:p.Arg458=
XM_011515841.1:c.1467A>G	XP_011514143.1:p.Arg489=
XM_011515842.1:c.1464A>G	XP_011514144.1:p.Arg488=
NM_017460.6:c.1374A>G MANE Select	NP_059488.2:p.Arg458=
NM_001202855.3:c.1371A>G	NP_001189784.1:p.Arg457=