Canonical Allele Identifier: CA368370682

Gene: CYP3A4

Linked Data

• dbSNP Id: rs2151558717
• gnomAD v4: 7-99768372-G-T
• MyVariant Identifiers: chr7:g.99365995G>T (hg19) ; chr7:g.99768372G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.99768372G>T , CM000669.2:g.99768372G>T	GRCh38
NC_000007.13:g.99365995G>T , CM000669.1:g.99365995G>T	GRCh37
NC_000007.12:g.99203931G>T	NCBI36
NG_008421.1:g.20814C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000336411.7:c.652C>A	ENSP00000337915.3:p.Pro218Thr
ENST00000651514.1:c.652C>A MANE Select	ENSP00000498939.1:p.Pro218Thr
ENST00000651783.1:c.193C>A	ENSP00000498924.1:p.Pro65Thr
ENST00000652018.1:c.505C>A	ENSP00000498733.1:p.Pro169Thr
ENST00000336411.6:c.652C>A	ENSP00000337915.2:p.Pro218Thr
ENST00000354593.6:c.202C>A	ENSP00000346607.2:p.Pro68Thr
NM_001202855.2:c.652C>A	NP_001189784.1:p.Pro218Thr
NM_017460.5:c.652C>A	NP_059488.2:p.Pro218Thr
XM_011515841.1:c.652C>A	XP_011514143.1:p.Pro218Thr
XM_011515842.1:c.652C>A	XP_011514144.1:p.Pro218Thr
NM_017460.6:c.652C>A MANE Select	NP_059488.2:p.Pro218Thr
NM_001202855.3:c.652C>A	NP_001189784.1:p.Pro218Thr