Canonical Allele Identifier: CA971510102

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063154050
• gnomAD v3: 15-74719790-G-A
• gnomAD v4: 15-74719790-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719790G>A , CM000677.2:g.74719790G>A	GRCh38
NC_000015.9:g.75012131G>A , CM000677.1:g.75012131G>A	GRCh37
NC_000015.8:g.72799184G>A	NCBI36
NG_008431.1:g.2249G>A
NG_008431.2:g.2249G>A
NG_061374.1:g.10739C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*699C>T MANE Select	ENSP00000369050.3:n.*699C>T
ENST00000379727.7:c.*699C>T	ENSP00000369050.3:n.*699C>T
ENST00000395048.6:c.*699C>T	ENSP00000378488.2:n.*699C>T
ENST00000612821.4:c.2154C>T	ENSP00000479744.1:n.2154C>T
ENST00000617691.4:c.*699C>T	ENSP00000482863.1:n.*699C>T
NM_000499.3:c.*699C>T	NP_000490.1:n.*699C>T
XM_005254185.1:c.*699C>T	XP_005254242.1:n.*699C>T
NM_000499.5:c.*699C>T	NP_000490.1:n.*699C>T
NM_001319216.2:c.*699C>T	NP_001306145.1:n.*699C>T
NM_001319217.2:c.*699C>T MANE Select	NP_001306146.1:n.*699C>T