Canonical Allele Identifier: CA619412556

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1475629559
• gnomAD v2: 15-75013167-A-G
• gnomAD v3: 15-74720826-A-G
• gnomAD v4: 15-74720826-A-G
• MyVariant Identifiers: chr15:g.75013167A>G (hg19) ; chr15:g.74720826A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720826A>G , CM000677.2:g.74720826A>G	GRCh38
NC_000015.9:g.75013167A>G , CM000677.1:g.75013167A>G	GRCh37
NC_000015.8:g.72800220A>G	NCBI36
NG_008431.1:g.3285A>G
NG_008431.2:g.3285A>G
NG_061374.1:g.9703T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1254-52T>C MANE Select	ENSP00000369050.3:n.1254-52T>C
ENST00000379727.7:c.1254-52T>C	ENSP00000369050.3:n.1254-52T>C
ENST00000395048.6:c.1254-52T>C	ENSP00000378488.2:n.1254-52T>C
ENST00000395049.8:c.1167-52T>C	ENSP00000378489.4:n.1167-52T>C
ENST00000562201.5:c.*491-52T>C	ENSP00000455340.1:n.*491-52T>C
ENST00000564596.5:c.*137T>C	ENSP00000457668.1:n.*137T>C
ENST00000566503.1:c.471-52T>C	ENSP00000455846.1:n.471-52T>C
ENST00000567032.5:c.1254-52T>C	ENSP00000456585.1:n.1254-52T>C
ENST00000569630.5:c.*843-52T>C	ENSP00000455051.1:n.*843-52T>C
ENST00000612821.4:c.1170-52T>C	ENSP00000479744.1:n.1170-52T>C
ENST00000617691.4:c.1167-52T>C	ENSP00000482863.1:n.1167-52T>C
NM_000499.3:c.1254-52T>C	NP_000490.1:n.1254-52T>C
XM_005254185.1:c.1254-52T>C	XP_005254242.1:n.1254-52T>C
NM_000499.5:c.1254-52T>C	NP_000490.1:n.1254-52T>C
NM_001319216.2:c.1167-52T>C	NP_001306145.1:n.1167-52T>C
NM_001319217.2:c.1254-52T>C MANE Select	NP_001306146.1:n.1254-52T>C