Canonical Allele Identifier: CA272812543

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1045022001
• gnomAD v3: 15-74719766-T-C
• gnomAD v4: 15-74719766-T-C
• MyVariant Identifiers: chr15:g.75012107T>C (hg19) ; chr15:g.74719766T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719766T>C , CM000677.2:g.74719766T>C	GRCh38
NC_000015.9:g.75012107T>C , CM000677.1:g.75012107T>C	GRCh37
NC_000015.8:g.72799160T>C	NCBI36
NG_008431.1:g.2225T>C
NG_008431.2:g.2225T>C
NG_061374.1:g.10763A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*723A>G MANE Select	ENSP00000369050.3:n.*723A>G
ENST00000379727.7:c.*723A>G	ENSP00000369050.3:n.*723A>G
ENST00000395048.6:c.*723A>G	ENSP00000378488.2:n.*723A>G
ENST00000612821.4:c.2178A>G	ENSP00000479744.1:n.2178A>G
ENST00000617691.4:c.*723A>G	ENSP00000482863.1:n.*723A>G
NM_000499.3:c.*723A>G	NP_000490.1:n.*723A>G
XM_005254185.1:c.*723A>G	XP_005254242.1:n.*723A>G
NM_000499.5:c.*723A>G	NP_000490.1:n.*723A>G
NM_001319216.2:c.*723A>G	NP_001306145.1:n.*723A>G
NM_001319217.2:c.*723A>G MANE Select	NP_001306146.1:n.*723A>G