Canonical Allele Identifier: CA163156866
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs12721634
MyVariant Identifiers: chr7:g.99381661A>G (hg19) chr7:g.99784038A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99784038A>G , CM000669.2:g.99784038A>G GRCh38
NC_000007.13:g.99381661A>G , CM000669.1:g.99381661A>G GRCh37
NC_000007.12:g.99219597A>G NCBI36
NG_008421.1:g.5148T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.44T>C ENSP00000337915.3:p.Leu15Pro
ENST00000651514.1:c.44T>C MANE Select ENSP00000498939.1:p.Leu15Pro
ENST00000652018.1:c.44T>C ENSP00000498733.1:p.Leu15Pro
ENST00000336411.6:c.44T>C ENSP00000337915.2:p.Leu15Pro
ENST00000354593.6:c.44T>C ENSP00000346607.2:p.Leu15Pro
ENST00000415003.1:c.44T>C ENSP00000397208.1:p.Leu15Pro
NM_001202855.2:c.44T>C NP_001189784.1:p.Leu15Pro
NM_017460.5:c.44T>C NP_059488.2:p.Leu15Pro
XM_011515841.1:c.44T>C XP_011514143.1:p.Leu15Pro
XM_011515842.1:c.44T>C XP_011514144.1:p.Leu15Pro
NM_017460.6:c.44T>C MANE Select NP_059488.2:p.Leu15Pro
NM_001202855.3:c.44T>C NP_001189784.1:p.Leu15Pro
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