Canonical Allele Identifier: CA4369932

Gene: CYP3A4

Linked Data

• dbSNP Id: rs778644522
• ExAC: 7:99381623 C / T
• gnomAD v2: 7-99381623-C-T
• gnomAD v4: 7-99784000-C-T
• MyVariant Identifiers: chr7:g.99381623C>T (hg19) ; chr7:g.99784000C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99784000C>T , CM000669.2:g.99784000C>T	GRCh38
NC_000007.13:g.99381623C>T , CM000669.1:g.99381623C>T	GRCh37
NC_000007.12:g.99219559C>T	NCBI36
NG_008421.1:g.5186G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.71+11G>A	ENSP00000337915.3:n.71+11G>A
ENST00000651514.1:c.71+11G>A MANE Select	ENSP00000498939.1:n.71+11G>A
ENST00000652018.1:c.71+11G>A	ENSP00000498733.1:n.71+11G>A
ENST00000336411.6:c.71+11G>A	ENSP00000337915.2:n.71+11G>A
ENST00000354593.6:c.71+11G>A	ENSP00000346607.2:n.71+11G>A
ENST00000415003.1:c.71+11G>A	ENSP00000397208.1:n.71+11G>A
NM_001202855.2:c.71+11G>A	NP_001189784.1:n.71+11G>A
NM_017460.5:c.71+11G>A	NP_059488.2:n.71+11G>A
XM_011515841.1:c.71+11G>A	XP_011514143.1:n.71+11G>A
XM_011515842.1:c.71+11G>A	XP_011514144.1:n.71+11G>A
NM_017460.6:c.71+11G>A MANE Select	NP_059488.2:n.71+11G>A
NM_001202855.3:c.71+11G>A	NP_001189784.1:n.71+11G>A