Canonical Allele Identifier: CA1729180222
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs1815504958
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99767478G>T , CM000669.2:g.99767478G>T GRCh38
NC_000007.13:g.99365101G>T , CM000669.1:g.99365101G>T GRCh37
NC_000007.12:g.99203037G>T NCBI36
NG_008421.1:g.21708C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.671-220C>A ENSP00000337915.3:n.671-220C>A
ENST00000651162.1:n.106-220C>A
ENST00000651514.1:c.671-220C>A MANE Select ENSP00000498939.1:n.671-220C>A
ENST00000651783.1:c.212-220C>A ENSP00000498924.1:n.212-220C>A
ENST00000652018.1:c.524-220C>A ENSP00000498733.1:n.524-220C>A
ENST00000336411.6:c.671-220C>A ENSP00000337915.2:n.671-220C>A
ENST00000354593.6:c.221-220C>A ENSP00000346607.2:n.221-220C>A
NM_001202855.2:c.671-223C>A NP_001189784.1:n.671-223C>A
NM_017460.5:c.671-220C>A NP_059488.2:n.671-220C>A
XM_011515841.1:c.671-220C>A XP_011514143.1:n.671-220C>A
XM_011515842.1:c.671-223C>A XP_011514144.1:n.671-223C>A
NM_017460.6:c.671-220C>A MANE Select NP_059488.2:n.671-220C>A
NM_001202855.3:c.671-223C>A NP_001189784.1:n.671-223C>A
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