Canonical Allele Identifier: CA456690204
Gene: CYP3A4 HGNC NCBI

Linked Data

gnomAD v4: 7-99769779-G-A
MyVariant Identifiers: chr7:g.99367402G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769779G>A , CM000669.2:g.99769779G>A GRCh38
NC_000007.13:g.99367402G>A , CM000669.1:g.99367402G>A GRCh37
NC_000007.12:g.99205338G>A NCBI36
NG_008421.1:g.19407C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.510C>T ENSP00000337915.3:p.Val170=
ENST00000651514.1:c.510C>T MANE Select ENSP00000498939.1:p.Val170=
ENST00000651783.1:c.58-1272C>T ENSP00000498924.1:n.58-1272C>T
ENST00000652018.1:c.363C>T ENSP00000498733.1:p.Val121=
ENST00000336411.6:c.510C>T ENSP00000337915.2:p.Val170=
ENST00000354593.6:c.72-1277C>T ENSP00000346607.2:n.72-1277C>T
ENST00000480043.1:n.407C>T
NM_001202855.2:c.510C>T NP_001189784.1:p.Val170=
NM_017460.5:c.510C>T NP_059488.2:p.Val170=
XM_011515841.1:c.510C>T XP_011514143.1:p.Val170=
XM_011515842.1:c.510C>T XP_011514144.1:p.Val170=
NM_017460.6:c.510C>T MANE Select NP_059488.2:p.Val170=
NM_001202855.3:c.510C>T NP_001189784.1:p.Val170=