Canonical Allele Identifier: CA971486887

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063203745
• gnomAD v3: 15-74724955-C-T
• gnomAD v4: 15-74724955-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74724955C>T , CM000677.2:g.74724955C>T	GRCh38
NC_000015.9:g.75017296C>T , CM000677.1:g.75017296C>T	GRCh37
NC_000015.8:g.72804349C>T	NCBI36
NG_008431.1:g.7414C>T
NG_008431.2:g.7414C>T
NG_061374.1:g.5574G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.-30+486G>A MANE Select	ENSP00000369050.3:n.-30+486G>A
ENST00000379727.7:c.-30+486G>A	ENSP00000369050.3:n.-30+486G>A
ENST00000395048.6:c.-27+486G>A	ENSP00000378488.2:n.-27+486G>A
ENST00000395049.8:c.-30+486G>A	ENSP00000378489.4:n.-30+486G>A
ENST00000562201.5:c.-27+486G>A	ENSP00000455340.1:n.-27+486G>A
ENST00000564596.5:c.-221+486G>A	ENSP00000457668.1:n.-221+486G>A
ENST00000566503.1:c.-221+486G>A	ENSP00000455846.1:n.-221+486G>A
ENST00000567032.5:c.-30+210G>A	ENSP00000456585.1:n.-30+210G>A
ENST00000569630.5:c.-27+486G>A	ENSP00000455051.1:n.-27+486G>A
ENST00000617691.4:c.-27+486G>A	ENSP00000482863.1:n.-27+486G>A
NM_000499.3:c.-27+486G>A	NP_000490.1:n.-27+486G>A
XM_005254185.1:c.-30+486G>A	XP_005254242.1:n.-30+486G>A
NM_000499.5:c.-27+486G>A	NP_000490.1:n.-27+486G>A
NM_001319216.2:c.-30+486G>A	NP_001306145.1:n.-30+486G>A
NM_001319217.2:c.-30+486G>A MANE Select	NP_001306146.1:n.-30+486G>A