Canonical Allele Identifier: CA4369700
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs3208361

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768447T>C , CM000669.2:g.99768447T>C GRCh38
NC_000007.13:g.99366070T>C , CM000669.1:g.99366070T>C GRCh37
NC_000007.12:g.99204006T>C NCBI36
NG_008421.1:g.20739A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.577A>G ENSP00000337915.3:p.Ile193Val
ENST00000651514.1:c.577A>G MANE Select ENSP00000498939.1:p.Ile193Val
ENST00000651783.1:n.118A>G ENSP00000498924.1:p.Ile40Val
ENST00000652018.1:c.430A>G ENSP00000498733.1:p.Ile144Val
ENST00000336411.6:c.577A>G ENSP00000337915.2:p.Ile193Val
ENST00000354593.6:c.127A>G ENSP00000346607.2:p.Ile43Val
NM_001202855.2:c.577A>G NP_001189784.1:p.Ile193Val
NM_017460.5:c.577A>G NP_059488.2:p.Ile193Val
XM_011515841.1:c.577A>G XP_011514143.1:p.Ile193Val
XM_011515842.1:c.577A>G XP_011514144.1:p.Ile193Val
NM_017460.6:c.577A>G MANE Select NP_059488.2:p.Ile193Val
NM_001202855.3:c.577A>G NP_001189784.1:p.Ile193Val