Canonical Allele Identifier: CA4369679
Gene: CYP3A4 HGNC NCBI

Linked Data

dbSNP Id: rs565580106
gnomAD v2: 7-99365978-T-C
gnomAD v3: 7-99768355-T-C
gnomAD v4: 7-99768355-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.99768355T>C , CM000669.2:g.99768355T>C GRCh38
NC_000007.13:g.99365978T>C , CM000669.1:g.99365978T>C GRCh37
NC_000007.12:g.99203914T>C NCBI36
NG_008421.1:g.20831A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000336411.7:c.669A>G ENSP00000337915.3:p.Ile223Met
ENST00000651514.1:c.669A>G MANE Select ENSP00000498939.1:p.Ile223Met
ENST00000651783.1:c.210A>G ENSP00000498924.1:p.Ile70Met
ENST00000652018.1:c.522A>G ENSP00000498733.1:p.Ile174Met
ENST00000336411.6:c.669A>G ENSP00000337915.2:p.Ile223Met
ENST00000354593.6:c.219A>G ENSP00000346607.2:p.Ile73Met
NM_001202855.2:c.669A>G NP_001189784.1:p.Ile223Met
NM_017460.5:c.669A>G NP_059488.2:p.Ile223Met
XM_011515841.1:c.669A>G XP_011514143.1:p.Ile223Met
XM_011515842.1:c.669A>G XP_011514144.1:p.Ile223Met
NM_017460.6:c.669A>G MANE Select NP_059488.2:p.Ile223Met
NM_001202855.3:c.669A>G NP_001189784.1:p.Ile223Met