Canonical Allele Identifier: CA368369318

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1341107338
• gnomAD v2: 7-99359803-T-C
• gnomAD v4: 7-99762180-T-C
• MyVariant Identifiers: chr7:g.99359803T>C (hg19) ; chr7:g.99762180T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762180T>C , CM000669.2:g.99762180T>C	GRCh38
NC_000007.13:g.99359803T>C , CM000669.1:g.99359803T>C	GRCh37
NC_000007.12:g.99197739T>C	NCBI36
NG_008421.1:g.27006A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1114A>G	ENSP00000337915.3:p.Arg372Gly
ENST00000651162.1:n.549A>G
ENST00000651514.1:c.1114A>G MANE Select	ENSP00000498939.1:p.Arg372Gly
ENST00000651783.1:c.655A>G	ENSP00000498924.1:p.Arg219Gly
ENST00000652018.1:c.967A>G	ENSP00000498733.1:p.Arg323Gly
ENST00000336411.6:c.1114A>G	ENSP00000337915.2:p.Arg372Gly
ENST00000354593.6:c.664A>G	ENSP00000346607.2:p.Arg222Gly
NM_001202855.2:c.1111A>G	NP_001189784.1:p.Arg371Gly
NM_017460.5:c.1114A>G	NP_059488.2:p.Arg372Gly
XM_011515841.1:c.1114A>G	XP_011514143.1:p.Arg372Gly
XM_011515842.1:c.1111A>G	XP_011514144.1:p.Arg371Gly
NM_017460.6:c.1114A>G MANE Select	NP_059488.2:p.Arg372Gly
NM_001202855.3:c.1111A>G	NP_001189784.1:p.Arg371Gly