Canonical Allele Identifier: CA2187814511

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1160055927

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719654A>G , CM000677.2:g.74719654A>G	GRCh38
NC_000015.9:g.75011995A>G , CM000677.1:g.75011995A>G	GRCh37
NC_000015.8:g.72799048A>G	NCBI36
NG_008431.1:g.2113A>G
NG_008431.2:g.2113A>G
NG_061374.1:g.10875T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*835T>C MANE Select	ENSP00000369050.3:n.*835T>C
ENST00000379727.7:c.*835T>C	ENSP00000369050.3:n.*835T>C
ENST00000395048.6:c.*835T>C	ENSP00000378488.2:n.*835T>C
ENST00000612821.4:c.2290T>C	ENSP00000479744.1:n.2290T>C
ENST00000617691.4:c.*835T>C	ENSP00000482863.1:n.*835T>C
NM_000499.3:c.*835T>C	NP_000490.1:n.*835T>C
XM_005254185.1:c.*835T>C	XP_005254242.1:n.*835T>C
NM_000499.5:c.*835T>C	NP_000490.1:n.*835T>C
NM_001319216.2:c.*835T>C	NP_001306145.1:n.*835T>C
NM_001319217.2:c.*835T>C MANE Select	NP_001306146.1:n.*835T>C