Canonical Allele Identifier: CA715665190
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs1179116997

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719821C>G , CM000677.2:g.74719821C>G GRCh38
NC_000015.9:g.75012162C>G , CM000677.1:g.75012162C>G GRCh37
NC_000015.8:g.72799215C>G NCBI36
NG_008431.1:g.2280C>G
NG_008431.2:g.2280C>G
NG_061374.1:g.10708G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*668G>C MANE Select ENSP00000369050.3:n.*668G>C
ENST00000379727.7:c.*668G>C ENSP00000369050.3:n.*668G>C
ENST00000395048.6:c.*668G>C ENSP00000378488.2:n.*668G>C
ENST00000612821.4:c.2123G>C ENSP00000479744.1:n.2123G>C
ENST00000617691.4:c.*668G>C ENSP00000482863.1:n.*668G>C
NM_000499.3:c.*668G>C NP_000490.1:n.*668G>C
XM_005254185.1:c.*668G>C XP_005254242.1:n.*668G>C
NM_000499.5:c.*668G>C NP_000490.1:n.*668G>C
NM_001319216.2:c.*668G>C NP_001306145.1:n.*668G>C
NM_001319217.2:c.*668G>C MANE Select NP_001306146.1:n.*668G>C