Canonical Allele Identifier: CA163153380

Gene: CYP3A4

Linked Data

• dbSNP Id: rs935043481
• gnomAD v3: 7-99768408-T-A
• gnomAD v4: 7-99768408-T-A
• MyVariant Identifiers: chr7:g.99366031T>A (hg19) ; chr7:g.99768408T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768408T>A , CM000669.2:g.99768408T>A	GRCh38
NC_000007.13:g.99366031T>A , CM000669.1:g.99366031T>A	GRCh37
NC_000007.12:g.99203967T>A	NCBI36
NG_008421.1:g.20778A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.616A>T	ENSP00000337915.3:p.Asn206Tyr
ENST00000651514.1:c.616A>T MANE Select	ENSP00000498939.1:p.Asn206Tyr
ENST00000651783.1:c.157A>T	ENSP00000498924.1:p.Asn53Tyr
ENST00000652018.1:c.469A>T	ENSP00000498733.1:p.Asn157Tyr
ENST00000336411.6:c.616A>T	ENSP00000337915.2:p.Asn206Tyr
ENST00000354593.6:c.166A>T	ENSP00000346607.2:p.Asn56Tyr
NM_001202855.2:c.616A>T	NP_001189784.1:p.Asn206Tyr
NM_017460.5:c.616A>T	NP_059488.2:p.Asn206Tyr
XM_011515841.1:c.616A>T	XP_011514143.1:p.Asn206Tyr
XM_011515842.1:c.616A>T	XP_011514144.1:p.Asn206Tyr
NM_017460.6:c.616A>T MANE Select	NP_059488.2:p.Asn206Tyr
NM_001202855.3:c.616A>T	NP_001189784.1:p.Asn206Tyr