Canonical Allele Identifier: CA456690143
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1563041764
MyVariant Identifiers: chr7:g.99366038A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768415A>G , CM000669.2:g.99768415A>G GRCh38
NC_000007.13:g.99366038A>G , CM000669.1:g.99366038A>G GRCh37
NC_000007.12:g.99203974A>G NCBI36
NG_008421.1:g.20771T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.609T>C ENSP00000337915.3:p.Phe203=
ENST00000651514.1:c.609T>C MANE Select ENSP00000498939.1:p.Phe203=
ENST00000651783.1:c.150T>C ENSP00000498924.1:p.Phe50=
ENST00000652018.1:c.462T>C ENSP00000498733.1:p.Phe154=
ENST00000336411.6:c.609T>C ENSP00000337915.2:p.Phe203=
ENST00000354593.6:c.159T>C ENSP00000346607.2:p.Phe53=
NM_001202855.2:c.609T>C NP_001189784.1:p.Phe203=
NM_017460.5:c.609T>C NP_059488.2:p.Phe203=
XM_011515841.1:c.609T>C XP_011514143.1:p.Phe203=
XM_011515842.1:c.609T>C XP_011514144.1:p.Phe203=
NM_017460.6:c.609T>C MANE Select NP_059488.2:p.Phe203=
NM_001202855.3:c.609T>C NP_001189784.1:p.Phe203=