Canonical Allele Identifier: CA393163884

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1387269151
• gnomAD v2: 15-75012904-C-A
• gnomAD v4: 15-74720563-C-A
• MyVariant Identifiers: chr15:g.75012904C>A (hg19) ; chr15:g.74720563C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720563C>A , CM000677.2:g.74720563C>A	GRCh38
NC_000015.9:g.75012904C>A , CM000677.1:g.75012904C>A	GRCh37
NC_000015.8:g.72799957C>A	NCBI36
NG_008431.1:g.3022C>A
NG_008431.2:g.3022C>A
NG_061374.1:g.9966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1465G>T MANE Select	ENSP00000369050.3:p.Asp489Tyr
ENST00000379727.7:c.1465G>T	ENSP00000369050.3:p.Asp489Tyr
ENST00000395048.6:c.1465G>T	ENSP00000378488.2:p.Asp489Tyr
ENST00000395049.8:c.1378G>T	ENSP00000378489.4:p.Asp460Tyr
ENST00000567032.5:c.1465G>T	ENSP00000456585.1:p.Asp489Tyr
ENST00000612821.4:c.1381G>T	ENSP00000479744.1:p.Asp461Tyr
ENST00000617691.4:c.1378G>T	ENSP00000482863.1:p.Asp460Tyr
NM_000499.3:c.1465G>T	NP_000490.1:p.Asp489Tyr
XM_005254185.1:c.1465G>T	XP_005254242.1:p.Asp489Tyr
NM_000499.5:c.1465G>T	NP_000490.1:p.Asp489Tyr
NM_001319216.2:c.1378G>T	NP_001306145.1:p.Asp460Tyr
NM_001319217.2:c.1465G>T MANE Select	NP_001306146.1:p.Asp489Tyr