Canonical Allele Identifier: CA4369514

Gene: CYP3A4

Linked Data

• dbSNP Id: rs750470018
• ExAC: 7:99358610 T / G
• gnomAD v3: 7-99760987-T-G
• gnomAD v4: 7-99760987-T-G
• MyVariant Identifiers: chr7:g.99358610T>G (hg19) ; chr7:g.99760987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760987T>G , CM000669.2:g.99760987T>G	GRCh38
NC_000007.13:g.99358610T>G , CM000669.1:g.99358610T>G	GRCh37
NC_000007.12:g.99196546T>G	NCBI36
NG_008421.1:g.28199A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1347-6A>C	ENSP00000337915.3:n.1347-6A>C
ENST00000651162.1:n.689-6A>C
ENST00000651514.1:c.1254-6A>C MANE Select	ENSP00000498939.1:n.1254-6A>C
ENST00000651783.1:c.795-6A>C	ENSP00000498924.1:n.795-6A>C
ENST00000652018.1:c.1107-6A>C	ENSP00000498733.1:n.1107-6A>C
ENST00000336411.6:c.1254-6A>C	ENSP00000337915.2:n.1254-6A>C
ENST00000354593.6:c.804-6A>C	ENSP00000346607.2:n.804-6A>C
NM_001202855.2:c.1251-6A>C	NP_001189784.1:n.1251-6A>C
NM_017460.5:c.1254-6A>C	NP_059488.2:n.1254-6A>C
XM_011515841.1:c.1347-6A>C	XP_011514143.1:n.1347-6A>C
XM_011515842.1:c.1344-6A>C	XP_011514144.1:n.1344-6A>C
NM_017460.6:c.1254-6A>C MANE Select	NP_059488.2:n.1254-6A>C
NM_001202855.3:c.1251-6A>C	NP_001189784.1:n.1251-6A>C