Canonical Allele Identifier: CA163153414

Gene: CYP3A4

Linked Data

• dbSNP Id: rs4987161
• gnomAD v3: 7-99768458-A-G
• gnomAD v4: 7-99768458-A-G
• MyVariant Identifiers: chr7:g.99366081A>G (hg19) ; chr7:g.99768458A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768458A>G , CM000669.2:g.99768458A>G	GRCh38
NC_000007.13:g.99366081A>G , CM000669.1:g.99366081A>G	GRCh37
NC_000007.12:g.99204017A>G	NCBI36
NG_008421.1:g.20728T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.566T>C	ENSP00000337915.3:p.Phe189Ser
ENST00000651514.1:c.566T>C MANE Select	ENSP00000498939.1:p.Phe189Ser
ENST00000651783.1:c.107T>C	ENSP00000498924.1:p.Phe36Ser
ENST00000652018.1:c.419T>C	ENSP00000498733.1:p.Phe140Ser
ENST00000336411.6:c.566T>C	ENSP00000337915.2:p.Phe189Ser
ENST00000354593.6:c.116T>C	ENSP00000346607.2:p.Phe39Ser
NM_001202855.2:c.566T>C	NP_001189784.1:p.Phe189Ser
NM_017460.5:c.566T>C	NP_059488.2:p.Phe189Ser
XM_011515841.1:c.566T>C	XP_011514143.1:p.Phe189Ser
XM_011515842.1:c.566T>C	XP_011514144.1:p.Phe189Ser
NM_017460.6:c.566T>C MANE Select	NP_059488.2:p.Phe189Ser
NM_001202855.3:c.566T>C	NP_001189784.1:p.Phe189Ser