Canonical Allele Identifier: CA272812531

Gene: CYP1A1

Linked Data

• dbSNP Id: rs556665867
• gnomAD v2: 15-75011978-A-G
• gnomAD v3: 15-74719637-A-G
• gnomAD v4: 15-74719637-A-G
• MyVariant Identifiers: chr15:g.75011978A>G (hg19) ; chr15:g.74719637A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719637A>G , CM000677.2:g.74719637A>G	GRCh38
NC_000015.9:g.75011978A>G , CM000677.1:g.75011978A>G	GRCh37
NC_000015.8:g.72799031A>G	NCBI36
NG_008431.1:g.2096A>G
NG_008431.2:g.2096A>G
NG_061374.1:g.10892T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*852T>C MANE Select	ENSP00000369050.3:n.*852T>C
ENST00000379727.7:c.*852T>C	ENSP00000369050.3:n.*852T>C
ENST00000395048.6:c.*852T>C	ENSP00000378488.2:n.*852T>C
ENST00000612821.4:c.2307T>C	ENSP00000479744.1:n.2307T>C
ENST00000617691.4:c.*852T>C	ENSP00000482863.1:n.*852T>C
NM_000499.3:c.*852T>C	NP_000490.1:n.*852T>C
XM_005254185.1:c.*852T>C	XP_005254242.1:n.*852T>C
NM_000499.5:c.*852T>C	NP_000490.1:n.*852T>C
NM_001319216.2:c.*852T>C	NP_001306145.1:n.*852T>C
NM_001319217.2:c.*852T>C MANE Select	NP_001306146.1:n.*852T>C