Canonical Allele Identifier: CA844515646

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1215406974
• gnomAD v4: 7-99769991-T-C
• MyVariant Identifiers: chr7:g.99367614T>C (hg19) ; chr7:g.99769991T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99769991T>C , CM000669.2:g.99769991T>C	GRCh38
NC_000007.13:g.99367614T>C , CM000669.1:g.99367614T>C	GRCh37
NC_000007.12:g.99205550T>C	NCBI36
NG_008421.1:g.19195A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.432+131A>G	ENSP00000337915.3:n.432+131A>G
ENST00000651514.1:c.432+131A>G MANE Select	ENSP00000498939.1:n.432+131A>G
ENST00000651783.1:c.58-1484A>G	ENSP00000498924.1:n.58-1484A>G
ENST00000652018.1:c.285+131A>G	ENSP00000498733.1:n.285+131A>G
ENST00000336411.6:c.432+131A>G	ENSP00000337915.2:n.432+131A>G
ENST00000354593.6:c.72-1489A>G	ENSP00000346607.2:n.72-1489A>G
ENST00000480043.1:n.329+131A>G
NM_001202855.2:c.432+131A>G	NP_001189784.1:n.432+131A>G
NM_017460.5:c.432+131A>G	NP_059488.2:n.432+131A>G
XM_011515841.1:c.432+131A>G	XP_011514143.1:n.432+131A>G
XM_011515842.1:c.432+131A>G	XP_011514144.1:n.432+131A>G
NM_017460.6:c.432+131A>G MANE Select	NP_059488.2:n.432+131A>G
NM_001202855.3:c.432+131A>G	NP_001189784.1:n.432+131A>G