Canonical Allele Identifier: CA272812571
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs4986883

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719876T>C , CM000677.2:g.74719876T>C GRCh38
NC_000015.9:g.75012217T>C , CM000677.1:g.75012217T>C GRCh37
NC_000015.8:g.72799270T>C NCBI36
NG_008431.1:g.2335T>C
NG_008431.2:g.2335T>C
NG_061374.1:g.10653A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*613A>G MANE Select ENSP00000369050.3:n.*613A>G
ENST00000379727.7:c.*613A>G ENSP00000369050.3:n.*613A>G
ENST00000395048.6:c.*613A>G ENSP00000378488.2:n.*613A>G
ENST00000612821.4:c.2068A>G ENSP00000479744.1:n.2068A>G
ENST00000617691.4:c.*613A>G ENSP00000482863.1:n.*613A>G
NM_000499.3:c.*613A>G NP_000490.1:n.*613A>G
XM_005254185.1:c.*613A>G XP_005254242.1:n.*613A>G
NM_000499.5:c.*613A>G NP_000490.1:n.*613A>G
NM_001319216.2:c.*613A>G NP_001306145.1:n.*613A>G
NM_001319217.2:c.*613A>G MANE Select NP_001306146.1:n.*613A>G