Canonical Allele Identifier: CA4369746
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs57409622
gnomAD v2: 7-99367428-G-A
gnomAD v3: 7-99769805-G-A
gnomAD v4: 7-99769805-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99769805G>A , CM000669.2:g.99769805G>A GRCh38
NC_000007.13:g.99367428G>A , CM000669.1:g.99367428G>A GRCh37
NC_000007.12:g.99205364G>A NCBI36
NG_008421.1:g.19381C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000336411.7:c.484C>T ENSP00000337915.3:p.Arg162Trp
ENST00000651514.1:c.484C>T MANE Select ENSP00000498939.1:p.Arg162Trp
ENST00000651783.1:c.58-1298C>T ENSP00000498924.1:n.58-1298C>T
ENST00000652018.1:c.337C>T ENSP00000498733.1:p.Arg113Trp
ENST00000336411.6:c.484C>T ENSP00000337915.2:p.Arg162Trp
ENST00000354593.6:c.72-1303C>T ENSP00000346607.2:n.72-1303C>T
ENST00000480043.1:n.381C>T
NM_001202855.2:c.484C>T NP_001189784.1:p.Arg162Trp
NM_017460.5:c.484C>T NP_059488.2:p.Arg162Trp
XM_011515841.1:c.484C>T XP_011514143.1:p.Arg162Trp
XM_011515842.1:c.484C>T XP_011514144.1:p.Arg162Trp
NM_017460.6:c.484C>T MANE Select NP_059488.2:p.Arg162Trp
NM_001202855.3:c.484C>T NP_001189784.1:p.Arg162Trp