Canonical Allele Identifier: CA456686626

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1397330819
• gnomAD v2: 7-99358547-A-G
• gnomAD v4: 7-99760924-A-G
• MyVariant Identifiers: chr7:g.99358547A>G (hg19) ; chr7:g.99760924A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99760924A>G , CM000669.2:g.99760924A>G	GRCh38
NC_000007.13:g.99358547A>G , CM000669.1:g.99358547A>G	GRCh37
NC_000007.12:g.99196483A>G	NCBI36
NG_008421.1:g.28262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336411.7:c.1404T>C	ENSP00000337915.3:p.Ser468=
ENST00000651162.1:n.746T>C
ENST00000651514.1:c.1311T>C MANE Select	ENSP00000498939.1:p.Ser437=
ENST00000651783.1:c.852T>C	ENSP00000498924.1:p.Ser284=
ENST00000652018.1:c.1164T>C	ENSP00000498733.1:p.Ser388=
ENST00000336411.6:c.1311T>C	ENSP00000337915.2:p.Ser437=
ENST00000354593.6:c.861T>C	ENSP00000346607.2:p.Ser287=
NM_001202855.2:c.1308T>C	NP_001189784.1:p.Ser436=
NM_017460.5:c.1311T>C	NP_059488.2:p.Ser437=
XM_011515841.1:c.1404T>C	XP_011514143.1:p.Ser468=
XM_011515842.1:c.1401T>C	XP_011514144.1:p.Ser467=
NM_017460.6:c.1311T>C MANE Select	NP_059488.2:p.Ser437=
NM_001202855.3:c.1308T>C	NP_001189784.1:p.Ser436=