Canonical Allele Identifier: CA163153063

Gene: CYP3A4

Linked Data

• dbSNP Id: rs866973023
• MyVariant Identifiers: chr7:g.99364765C>T (hg19) ; chr7:g.99767142C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767142C>T , CM000669.2:g.99767142C>T	GRCh38
NC_000007.13:g.99364765C>T , CM000669.1:g.99364765C>T	GRCh37
NC_000007.12:g.99202701C>T	NCBI36
NG_008421.1:g.22044G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.787G>A	ENSP00000337915.3:p.Asp263Asn
ENST00000651162.1:n.222G>A
ENST00000651514.1:c.787G>A MANE Select	ENSP00000498939.1:p.Asp263Asn
ENST00000651783.1:c.328G>A	ENSP00000498924.1:p.Asp110Asn
ENST00000652018.1:c.640G>A	ENSP00000498733.1:p.Asp214Asn
ENST00000336411.6:c.787G>A	ENSP00000337915.2:p.Asp263Asn
ENST00000354593.6:c.337G>A	ENSP00000346607.2:p.Asp113Asn
NM_001202855.2:c.784G>A	NP_001189784.1:p.Asp262Asn
NM_017460.5:c.787G>A	NP_059488.2:p.Asp263Asn
XM_011515841.1:c.787G>A	XP_011514143.1:p.Asp263Asn
XM_011515842.1:c.784G>A	XP_011514144.1:p.Asp262Asn
NM_017460.6:c.787G>A MANE Select	NP_059488.2:p.Asp263Asn
NM_001202855.3:c.784G>A	NP_001189784.1:p.Asp262Asn