Canonical Allele Identifier: CA456690145

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1223993603
• gnomAD v2: 7-99366041-G-C
• gnomAD v4: 7-99768418-G-C
• MyVariant Identifiers: chr7:g.99366041G>C (hg19) ; chr7:g.99768418G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768418G>C , CM000669.2:g.99768418G>C	GRCh38
NC_000007.13:g.99366041G>C , CM000669.1:g.99366041G>C	GRCh37
NC_000007.12:g.99203977G>C	NCBI36
NG_008421.1:g.20768C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.606C>G	ENSP00000337915.3:p.Pro202=
ENST00000651514.1:c.606C>G MANE Select	ENSP00000498939.1:p.Pro202=
ENST00000651783.1:c.147C>G	ENSP00000498924.1:p.Pro49=
ENST00000652018.1:c.459C>G	ENSP00000498733.1:p.Pro153=
ENST00000336411.6:c.606C>G	ENSP00000337915.2:p.Pro202=
ENST00000354593.6:c.156C>G	ENSP00000346607.2:p.Pro52=
NM_001202855.2:c.606C>G	NP_001189784.1:p.Pro202=
NM_017460.5:c.606C>G	NP_059488.2:p.Pro202=
XM_011515841.1:c.606C>G	XP_011514143.1:p.Pro202=
XM_011515842.1:c.606C>G	XP_011514144.1:p.Pro202=
NM_017460.6:c.606C>G MANE Select	NP_059488.2:p.Pro202=
NM_001202855.3:c.606C>G	NP_001189784.1:p.Pro202=