Canonical Allele Identifier: CA368370626

Gene: CYP3A4

Linked Data

• dbSNP Id: rs55785340
• gnomAD v3: 7-99768360-A-T
• gnomAD v4: 7-99768360-A-T
• MyVariant Identifiers: chr7:g.99365983A>T (hg19) ; chr7:g.99768360A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768360A>T , CM000669.2:g.99768360A>T	GRCh38
NC_000007.13:g.99365983A>T , CM000669.1:g.99365983A>T	GRCh37
NC_000007.12:g.99203919A>T	NCBI36
NG_008421.1:g.20826T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.664T>A	ENSP00000337915.3:p.Ser222Thr
ENST00000651514.1:c.664T>A MANE Select	ENSP00000498939.1:p.Ser222Thr
ENST00000651783.1:c.205T>A	ENSP00000498924.1:p.Ser69Thr
ENST00000652018.1:c.517T>A	ENSP00000498733.1:p.Ser173Thr
ENST00000336411.6:c.664T>A	ENSP00000337915.2:p.Ser222Thr
ENST00000354593.6:c.214T>A	ENSP00000346607.2:p.Ser72Thr
NM_001202855.2:c.664T>A	NP_001189784.1:p.Ser222Thr
NM_017460.5:c.664T>A	NP_059488.2:p.Ser222Thr
XM_011515841.1:c.664T>A	XP_011514143.1:p.Ser222Thr
XM_011515842.1:c.664T>A	XP_011514144.1:p.Ser222Thr
NM_017460.6:c.664T>A MANE Select	NP_059488.2:p.Ser222Thr
NM_001202855.3:c.664T>A	NP_001189784.1:p.Ser222Thr