Canonical Allele Identifier: CA576401939
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1459320199
gnomAD v2: 7-99365951-A-G
gnomAD v4: 7-99768328-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768328A>G , CM000669.2:g.99768328A>G GRCh38
NC_000007.13:g.99365951A>G , CM000669.1:g.99365951A>G GRCh37
NC_000007.12:g.99203887A>G NCBI36
NG_008421.1:g.20858T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.670+26T>C ENSP00000337915.3:n.670+26T>C
ENST00000651514.1:c.670+26T>C MANE Select ENSP00000498939.1:n.670+26T>C
ENST00000651783.1:c.211+26T>C ENSP00000498924.1:n.211+26T>C
ENST00000652018.1:c.523+26T>C ENSP00000498733.1:n.523+26T>C
ENST00000336411.6:c.670+26T>C ENSP00000337915.2:n.670+26T>C
ENST00000354593.6:c.220+26T>C ENSP00000346607.2:n.220+26T>C
NM_001202855.2:c.670+26T>C NP_001189784.1:n.670+26T>C
NM_017460.5:c.670+26T>C NP_059488.2:n.670+26T>C
XM_011515841.1:c.670+26T>C XP_011514143.1:n.670+26T>C
XM_011515842.1:c.670+26T>C XP_011514144.1:n.670+26T>C
NM_017460.6:c.670+26T>C MANE Select NP_059488.2:n.670+26T>C
NM_001202855.3:c.670+26T>C NP_001189784.1:n.670+26T>C