Canonical Allele Identifier: CA2187816856

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063203098

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74724875T>C , CM000677.2:g.74724875T>C	GRCh38
NC_000015.9:g.75017216T>C , CM000677.1:g.75017216T>C	GRCh37
NC_000015.8:g.72804269T>C	NCBI36
NG_008431.1:g.7334T>C
NG_008431.2:g.7334T>C
NG_061374.1:g.5654A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.-30+566A>G MANE Select	ENSP00000369050.3:n.-30+566A>G
ENST00000379727.7:c.-30+566A>G	ENSP00000369050.3:n.-30+566A>G
ENST00000395048.6:c.-27+566A>G	ENSP00000378488.2:n.-27+566A>G
ENST00000395049.8:c.-30+566A>G	ENSP00000378489.4:n.-30+566A>G
ENST00000562201.5:c.-27+566A>G	ENSP00000455340.1:n.-27+566A>G
ENST00000564596.5:c.-221+566A>G	ENSP00000457668.1:n.-221+566A>G
ENST00000566503.1:c.-221+566A>G	ENSP00000455846.1:n.-221+566A>G
ENST00000567032.5:c.-30+290A>G	ENSP00000456585.1:n.-30+290A>G
ENST00000569630.5:c.-27+566A>G	ENSP00000455051.1:n.-27+566A>G
ENST00000617691.4:c.-27+566A>G	ENSP00000482863.1:n.-27+566A>G
NM_000499.3:c.-27+566A>G	NP_000490.1:n.-27+566A>G
XM_005254185.1:c.-30+566A>G	XP_005254242.1:n.-30+566A>G
NM_000499.5:c.-27+566A>G	NP_000490.1:n.-27+566A>G
NM_001319216.2:c.-30+566A>G	NP_001306145.1:n.-30+566A>G
NM_001319217.2:c.-30+566A>G MANE Select	NP_001306146.1:n.-30+566A>G