Canonical Allele Identifier: CA368369342

Gene: CYP3A4

Linked Data

• dbSNP Id: rs1309748501
• gnomAD v2: 7-99359808-G-A
• gnomAD v3: 7-99762185-G-A
• gnomAD v4: 7-99762185-G-A
• COSMIC: COSM274723
• MyVariant Identifiers: chr7:g.99359808G>A (hg19) ; chr7:g.99762185G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99762185G>A , CM000669.2:g.99762185G>A	GRCh38
NC_000007.13:g.99359808G>A , CM000669.1:g.99359808G>A	GRCh37
NC_000007.12:g.99197744G>A	NCBI36
NG_008421.1:g.27001C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.1109C>T	ENSP00000337915.3:p.Ala370Val
ENST00000651162.1:n.544C>T
ENST00000651514.1:c.1109C>T MANE Select	ENSP00000498939.1:p.Ala370Val
ENST00000651783.1:c.650C>T	ENSP00000498924.1:p.Ala217Val
ENST00000652018.1:c.962C>T	ENSP00000498733.1:p.Ala321Val
ENST00000336411.6:c.1109C>T	ENSP00000337915.2:p.Ala370Val
ENST00000354593.6:c.659C>T	ENSP00000346607.2:p.Ala220Val
NM_001202855.2:c.1106C>T	NP_001189784.1:p.Ala369Val
NM_017460.5:c.1109C>T	NP_059488.2:p.Ala370Val
XM_011515841.1:c.1109C>T	XP_011514143.1:p.Ala370Val
XM_011515842.1:c.1106C>T	XP_011514144.1:p.Ala369Val
NM_017460.6:c.1109C>T MANE Select	NP_059488.2:p.Ala370Val
NM_001202855.3:c.1106C>T	NP_001189784.1:p.Ala369Val