Canonical Allele Identifier: CA272812572

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1800031
• gnomAD v4: 15-74719894-A-G
• MyVariant Identifiers: chr15:g.75012235A>G (hg19) ; chr15:g.74719894A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719894A>G , CM000677.2:g.74719894A>G	GRCh38
NC_000015.9:g.75012235A>G , CM000677.1:g.75012235A>G	GRCh37
NC_000015.8:g.72799288A>G	NCBI36
NG_008431.1:g.2353A>G
NG_008431.2:g.2353A>G
NG_061374.1:g.10635T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.*595T>C MANE Select	ENSP00000369050.3:n.*595T>C
ENST00000379727.7:c.*595T>C	ENSP00000369050.3:n.*595T>C
ENST00000395048.6:c.*595T>C	ENSP00000378488.2:n.*595T>C
ENST00000612821.4:c.2050T>C	ENSP00000479744.1:n.2050T>C
ENST00000617691.4:c.*595T>C	ENSP00000482863.1:n.*595T>C
NM_000499.3:c.*595T>C	NP_000490.1:n.*595T>C
XM_005254185.1:c.*595T>C	XP_005254242.1:n.*595T>C
NM_000499.5:c.*595T>C	NP_000490.1:n.*595T>C
NM_001319216.2:c.*595T>C	NP_001306145.1:n.*595T>C
NM_001319217.2:c.*595T>C MANE Select	NP_001306146.1:n.*595T>C