Canonical Allele Identifier: CA368371182
Gene: CYP3A4 HGNC NCBI

Linked Data

gnomAD v4: 7-99768461-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768461G>T , CM000669.2:g.99768461G>T GRCh38
NC_000007.13:g.99366084G>T , CM000669.1:g.99366084G>T GRCh37
NC_000007.12:g.99204020G>T NCBI36
NG_008421.1:g.20725C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.563C>A ENSP00000337915.3:p.Ser188Ter
ENST00000651514.1:c.563C>A MANE Select ENSP00000498939.1:p.Ser188Ter
ENST00000651783.1:c.104C>A ENSP00000498924.1:p.Ser35Ter
ENST00000652018.1:c.416C>A ENSP00000498733.1:p.Ser139Ter
ENST00000336411.6:c.563C>A ENSP00000337915.2:p.Ser188Ter
ENST00000354593.6:c.113C>A ENSP00000346607.2:p.Ser38Ter
NM_001202855.2:c.563C>A NP_001189784.1:p.Ser188Ter
NM_017460.5:c.563C>A NP_059488.2:p.Ser188Ter
XM_011515841.1:c.563C>A XP_011514143.1:p.Ser188Ter
XM_011515842.1:c.563C>A XP_011514144.1:p.Ser188Ter
NM_017460.6:c.563C>A MANE Select NP_059488.2:p.Ser188Ter
NM_001202855.3:c.563C>A NP_001189784.1:p.Ser188Ter