Canonical Allele Identifier: CA2187814837

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063158038
• gnomAD v4: 15-74720454-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720454G>A , CM000677.2:g.74720454G>A	GRCh38
NC_000015.9:g.75012795G>A , CM000677.1:g.75012795G>A	GRCh37
NC_000015.8:g.72799848G>A	NCBI36
NG_008431.1:g.2913G>A
NG_008431.2:g.2913G>A
NG_061374.1:g.10075C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*35C>T MANE Select	ENSP00000369050.3:n.*35C>T
ENST00000379727.7:c.*35C>T	ENSP00000369050.3:n.*35C>T
ENST00000395048.6:c.*35C>T	ENSP00000378488.2:n.*35C>T
ENST00000395049.8:c.*35C>T	ENSP00000378489.4:n.*35C>T
ENST00000567032.5:c.*35C>T	ENSP00000456585.1:n.*35C>T
ENST00000612821.4:c.1490C>T	ENSP00000479744.1:n.1490C>T
ENST00000617691.4:c.*35C>T	ENSP00000482863.1:n.*35C>T
NM_000499.3:c.*35C>T	NP_000490.1:n.*35C>T
XM_005254185.1:c.*35C>T	XP_005254242.1:n.*35C>T
NM_000499.5:c.*35C>T	NP_000490.1:n.*35C>T
NM_001319216.2:c.*35C>T	NP_001306145.1:n.*35C>T
NM_001319217.2:c.*35C>T MANE Select	NP_001306146.1:n.*35C>T