Canonical Allele Identifier: CA715666975

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1379806329
• gnomAD v3: 15-74724874-A-G
• gnomAD v4: 15-74724874-A-G
• MyVariant Identifiers: chr15:g.75017215A>G (hg19) ; chr15:g.74724874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74724874A>G , CM000677.2:g.74724874A>G	GRCh38
NC_000015.9:g.75017215A>G , CM000677.1:g.75017215A>G	GRCh37
NC_000015.8:g.72804268A>G	NCBI36
NG_008431.1:g.7333A>G
NG_008431.2:g.7333A>G
NG_061374.1:g.5655T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.-30+567T>C MANE Select	ENSP00000369050.3:n.-30+567T>C
ENST00000379727.7:c.-30+567T>C	ENSP00000369050.3:n.-30+567T>C
ENST00000395048.6:c.-27+567T>C	ENSP00000378488.2:n.-27+567T>C
ENST00000395049.8:c.-30+567T>C	ENSP00000378489.4:n.-30+567T>C
ENST00000562201.5:c.-27+567T>C	ENSP00000455340.1:n.-27+567T>C
ENST00000564596.5:c.-221+567T>C	ENSP00000457668.1:n.-221+567T>C
ENST00000566503.1:c.-221+567T>C	ENSP00000455846.1:n.-221+567T>C
ENST00000567032.5:c.-30+291T>C	ENSP00000456585.1:n.-30+291T>C
ENST00000569630.5:c.-27+567T>C	ENSP00000455051.1:n.-27+567T>C
ENST00000617691.4:c.-27+567T>C	ENSP00000482863.1:n.-27+567T>C
NM_000499.3:c.-27+567T>C	NP_000490.1:n.-27+567T>C
XM_005254185.1:c.-30+567T>C	XP_005254242.1:n.-30+567T>C
NM_000499.5:c.-27+567T>C	NP_000490.1:n.-27+567T>C
NM_001319216.2:c.-30+567T>C	NP_001306145.1:n.-30+567T>C
NM_001319217.2:c.-30+567T>C MANE Select	NP_001306146.1:n.-30+567T>C