Canonical Allele Identifier: CA163153667

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1010752867
• gnomAD v3: 7-99769353-G-T
• gnomAD v4: 7-99769353-G-T
• MyVariant Identifiers: chr7:g.99366976G>T (hg19) ; chr7:g.99769353G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769353G>T , CM000669.2:g.99769353G>T	GRCh38
NC_000007.13:g.99366976G>T , CM000669.1:g.99366976G>T	GRCh37
NC_000007.12:g.99204912G>T	NCBI36
NG_008421.1:g.19833C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.521+415C>A	ENSP00000337915.3:n.521+415C>A
ENST00000651514.1:c.521+415C>A MANE Select	ENSP00000498939.1:n.521+415C>A
ENST00000651783.1:c.58-846C>A	ENSP00000498924.1:n.58-846C>A
ENST00000652018.1:c.374+415C>A	ENSP00000498733.1:n.374+415C>A
ENST00000336411.6:c.521+415C>A	ENSP00000337915.2:n.521+415C>A
ENST00000354593.6:c.72-851C>A	ENSP00000346607.2:n.72-851C>A
NM_001202855.2:c.521+415C>A	NP_001189784.1:n.521+415C>A
NM_017460.5:c.521+415C>A	NP_059488.2:n.521+415C>A
XM_011515841.1:c.521+415C>A	XP_011514143.1:n.521+415C>A
XM_011515842.1:c.521+415C>A	XP_011514144.1:n.521+415C>A
NM_017460.6:c.521+415C>A MANE Select	NP_059488.2:n.521+415C>A
NM_001202855.3:c.521+415C>A	NP_001189784.1:n.521+415C>A