Canonical Allele Identifier: CA456690152

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1474207867
• gnomAD v2: 7-99366053-A-G
• gnomAD v4: 7-99768430-A-G
• MyVariant Identifiers: chr7:g.99366053A>G (hg19) ; chr7:g.99768430A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768430A>G , CM000669.2:g.99768430A>G	GRCh38
NC_000007.13:g.99366053A>G , CM000669.1:g.99366053A>G	GRCh37
NC_000007.12:g.99203989A>G	NCBI36
NG_008421.1:g.20756T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.594T>C	ENSP00000337915.3:p.Asn198=
ENST00000651514.1:c.594T>C MANE Select	ENSP00000498939.1:p.Asn198=
ENST00000651783.1:c.135T>C	ENSP00000498924.1:p.Asn45=
ENST00000652018.1:c.447T>C	ENSP00000498733.1:p.Asn149=
ENST00000336411.6:c.594T>C	ENSP00000337915.2:p.Asn198=
ENST00000354593.6:c.144T>C	ENSP00000346607.2:p.Asn48=
NM_001202855.2:c.594T>C	NP_001189784.1:p.Asn198=
NM_017460.5:c.594T>C	NP_059488.2:p.Asn198=
XM_011515841.1:c.594T>C	XP_011514143.1:p.Asn198=
XM_011515842.1:c.594T>C	XP_011514144.1:p.Asn198=
NM_017460.6:c.594T>C MANE Select	NP_059488.2:p.Asn198=
NM_001202855.3:c.594T>C	NP_001189784.1:p.Asn198=