Canonical Allele Identifier: CA272812617

Gene: CYP1A1

Linked Data

• dbSNP Id: rs4986880
• gnomAD v2: 15-75012644-G-A
• gnomAD v3: 15-74720303-G-A
• gnomAD v4: 15-74720303-G-A
• MyVariant Identifiers: chr15:g.75012644G>A (hg19) ; chr15:g.74720303G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720303G>A , CM000677.2:g.74720303G>A	GRCh38
NC_000015.9:g.75012644G>A , CM000677.1:g.75012644G>A	GRCh37
NC_000015.8:g.72799697G>A	NCBI36
NG_008431.1:g.2762G>A
NG_008431.2:g.2762G>A
NG_061374.1:g.10226C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*186C>T MANE Select	ENSP00000369050.3:n.*186C>T
ENST00000379727.7:c.*186C>T	ENSP00000369050.3:n.*186C>T
ENST00000395048.6:c.*186C>T	ENSP00000378488.2:n.*186C>T
ENST00000567032.5:c.*186C>T	ENSP00000456585.1:n.*186C>T
ENST00000612821.4:c.1641C>T	ENSP00000479744.1:n.1641C>T
ENST00000617691.4:c.*186C>T	ENSP00000482863.1:n.*186C>T
NM_000499.3:c.*186C>T	NP_000490.1:n.*186C>T
XM_005254185.1:c.*186C>T	XP_005254242.1:n.*186C>T
NM_000499.5:c.*186C>T	NP_000490.1:n.*186C>T
NM_001319216.2:c.*186C>T	NP_001306145.1:n.*186C>T
NM_001319217.2:c.*186C>T MANE Select	NP_001306146.1:n.*186C>T