Canonical Allele Identifier: CA163153077
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs3208363
gnomAD v4: 7-99767175-A-T
MyVariant Identifiers: chr7:g.99364798A>T (hg19) chr7:g.99767175A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767175A>T , CM000669.2:g.99767175A>T GRCh38
NC_000007.13:g.99364798A>T , CM000669.1:g.99364798A>T GRCh37
NC_000007.12:g.99202734A>T NCBI36
NG_008421.1:g.22011T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.754T>A ENSP00000337915.3:p.Ser252Thr
ENST00000651162.1:n.189T>A
ENST00000651514.1:c.754T>A MANE Select ENSP00000498939.1:p.Ser252Thr
ENST00000651783.1:c.295T>A ENSP00000498924.1:p.Ser99Thr
ENST00000652018.1:c.607T>A ENSP00000498733.1:p.Ser203Thr
ENST00000336411.6:c.754T>A ENSP00000337915.2:p.Ser252Thr
ENST00000354593.6:c.304T>A ENSP00000346607.2:p.Ser102Thr
NM_001202855.2:c.751T>A NP_001189784.1:p.Ser251Thr
NM_017460.5:c.754T>A NP_059488.2:p.Ser252Thr
XM_011515841.1:c.754T>A XP_011514143.1:p.Ser252Thr
XM_011515842.1:c.751T>A XP_011514144.1:p.Ser251Thr
NM_017460.6:c.754T>A MANE Select NP_059488.2:p.Ser252Thr
NM_001202855.3:c.751T>A NP_001189784.1:p.Ser251Thr
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