Canonical Allele Identifier: CA456689847

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1815497658
• gnomAD v3: 7-99767212-A-G
• gnomAD v4: 7-99767212-A-G
• MyVariant Identifiers: chr7:g.99364835A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99767212A>G , CM000669.2:g.99767212A>G	GRCh38
NC_000007.13:g.99364835A>G , CM000669.1:g.99364835A>G	GRCh37
NC_000007.12:g.99202771A>G	NCBI36
NG_008421.1:g.21974T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.717T>C	ENSP00000337915.3:p.Cys239=
ENST00000651162.1:n.152T>C
ENST00000651514.1:c.717T>C MANE Select	ENSP00000498939.1:p.Cys239=
ENST00000651783.1:c.258T>C	ENSP00000498924.1:p.Cys86=
ENST00000652018.1:c.570T>C	ENSP00000498733.1:p.Cys190=
ENST00000336411.6:c.717T>C	ENSP00000337915.2:p.Cys239=
ENST00000354593.6:c.267T>C	ENSP00000346607.2:p.Cys89=
NM_001202855.2:c.714T>C	NP_001189784.1:p.Cys238=
NM_017460.5:c.717T>C	NP_059488.2:p.Cys239=
XM_011515841.1:c.717T>C	XP_011514143.1:p.Cys239=
XM_011515842.1:c.714T>C	XP_011514144.1:p.Cys238=
NM_017460.6:c.717T>C MANE Select	NP_059488.2:p.Cys239=
NM_001202855.3:c.714T>C	NP_001189784.1:p.Cys238=