Canonical Allele Identifier: CA16309263
Gene: CYP3A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1327418
ClinVar RCV Id: RCV001787698
dbSNP Id: rs4646437
gnomAD v2: 7-99365083-G-A
gnomAD v3: 7-99767460-G-A
gnomAD v4: 7-99767460-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767460G>A , CM000669.2:g.99767460G>A GRCh38
NC_000007.13:g.99365083G>A , CM000669.1:g.99365083G>A GRCh37
NC_000007.12:g.99203019G>A NCBI36
NG_008421.1:g.21726C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.671-202C>T ENSP00000337915.3:n.671-202C>T
ENST00000651162.1:n.106-202C>T
ENST00000651514.1:c.671-202C>T MANE Select ENSP00000498939.1:n.671-202C>T
ENST00000651783.1:c.212-202C>T ENSP00000498924.1:n.212-202C>T
ENST00000652018.1:c.524-202C>T ENSP00000498733.1:n.524-202C>T
ENST00000336411.6:c.671-202C>T ENSP00000337915.2:n.671-202C>T
ENST00000354593.6:c.221-202C>T ENSP00000346607.2:n.221-202C>T
NM_001202855.2:c.671-205C>T NP_001189784.1:n.671-205C>T
NM_017460.5:c.671-202C>T NP_059488.2:n.671-202C>T
XM_011515841.1:c.671-202C>T XP_011514143.1:n.671-202C>T
XM_011515842.1:c.671-205C>T XP_011514144.1:n.671-205C>T
NM_017460.6:c.671-202C>T MANE Select NP_059488.2:n.671-202C>T
NM_001202855.3:c.671-205C>T NP_001189784.1:n.671-205C>T