Canonical Allele Identifier: CA491488352

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1167632896
• gnomAD v2: 15-75013076-C-T
• gnomAD v4: 15-74720735-C-T
• MyVariant Identifiers: chr15:g.75013076C>T (hg19) ; chr15:g.74720735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720735C>T , CM000677.2:g.74720735C>T	GRCh38
NC_000015.9:g.75013076C>T , CM000677.1:g.75013076C>T	GRCh37
NC_000015.8:g.72800129C>T	NCBI36
NG_008431.1:g.3194C>T
NG_008431.2:g.3194C>T
NG_061374.1:g.9794G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1293G>A MANE Select	ENSP00000369050.3:p.Arg431=
ENST00000379727.7:c.1293G>A	ENSP00000369050.3:p.Arg431=
ENST00000395048.6:c.1293G>A	ENSP00000378488.2:p.Arg431=
ENST00000395049.8:c.1206G>A	ENSP00000378489.4:p.Arg402=
ENST00000562201.5:c.*530G>A	ENSP00000455340.1:n.*530G>A
ENST00000564596.5:c.*228G>A	ENSP00000457668.1:n.*228G>A
ENST00000566503.1:c.510G>A	ENSP00000455846.1:p.Arg170=
ENST00000567032.5:c.1293G>A	ENSP00000456585.1:p.Arg431=
ENST00000569630.5:c.*882G>A	ENSP00000455051.1:n.*882G>A
ENST00000612821.4:c.1209G>A	ENSP00000479744.1:p.Arg403=
ENST00000617691.4:c.1206G>A	ENSP00000482863.1:p.Arg402=
NM_000499.3:c.1293G>A	NP_000490.1:p.Arg431=
XM_005254185.1:c.1293G>A	XP_005254242.1:p.Arg431=
NM_000499.5:c.1293G>A	NP_000490.1:p.Arg431=
NM_001319216.2:c.1206G>A	NP_001306145.1:p.Arg402=
NM_001319217.2:c.1293G>A MANE Select	NP_001306146.1:p.Arg431=