Canonical Allele Identifier: CA715665139

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1382826476
• MyVariant Identifiers: chr15:g.75011948G>C (hg19) ; chr15:g.74719607G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719607G>C , CM000677.2:g.74719607G>C	GRCh38
NC_000015.9:g.75011948G>C , CM000677.1:g.75011948G>C	GRCh37
NC_000015.8:g.72799001G>C	NCBI36
NG_008431.1:g.2066G>C
NG_008431.2:g.2066G>C
NG_061374.1:g.10922C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*882C>G MANE Select	ENSP00000369050.3:n.*882C>G
ENST00000379727.7:c.*882C>G	ENSP00000369050.3:n.*882C>G
ENST00000395048.6:c.*882C>G	ENSP00000378488.2:n.*882C>G
ENST00000612821.4:c.2337C>G	ENSP00000479744.1:n.2337C>G
ENST00000617691.4:c.*882C>G	ENSP00000482863.1:n.*882C>G
NM_000499.3:c.*882C>G	NP_000490.1:n.*882C>G
XM_005254185.1:c.*882C>G	XP_005254242.1:n.*882C>G
NM_000499.5:c.*882C>G	NP_000490.1:n.*882C>G
NM_001319216.2:c.*882C>G	NP_001306145.1:n.*882C>G
NM_001319217.2:c.*882C>G MANE Select	NP_001306146.1:n.*882C>G