Canonical Allele Identifier: CA272812644

Gene: CYP1A1

Linked Data

• dbSNP Id: rs973901273
• MyVariant Identifiers: chr15:g.75013126A>C (hg19) ; chr15:g.74720785A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720785A>C , CM000677.2:g.74720785A>C	GRCh38
NC_000015.9:g.75013126A>C , CM000677.1:g.75013126A>C	GRCh37
NC_000015.8:g.72800179A>C	NCBI36
NG_008431.1:g.3244A>C
NG_008431.2:g.3244A>C
NG_061374.1:g.9744T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1254-11T>G MANE Select	ENSP00000369050.3:n.1254-11T>G
ENST00000379727.7:c.1254-11T>G	ENSP00000369050.3:n.1254-11T>G
ENST00000395048.6:c.1254-11T>G	ENSP00000378488.2:n.1254-11T>G
ENST00000395049.8:c.1167-11T>G	ENSP00000378489.4:n.1167-11T>G
ENST00000562201.5:c.*491-11T>G	ENSP00000455340.1:n.*491-11T>G
ENST00000564596.5:c.*178T>G	ENSP00000457668.1:n.*178T>G
ENST00000566503.1:c.471-11T>G	ENSP00000455846.1:n.471-11T>G
ENST00000567032.5:c.1254-11T>G	ENSP00000456585.1:n.1254-11T>G
ENST00000569630.5:c.*843-11T>G	ENSP00000455051.1:n.*843-11T>G
ENST00000612821.4:c.1170-11T>G	ENSP00000479744.1:n.1170-11T>G
ENST00000617691.4:c.1167-11T>G	ENSP00000482863.1:n.1167-11T>G
NM_000499.3:c.1254-11T>G	NP_000490.1:n.1254-11T>G
XM_005254185.1:c.1254-11T>G	XP_005254242.1:n.1254-11T>G
NM_000499.5:c.1254-11T>G	NP_000490.1:n.1254-11T>G
NM_001319216.2:c.1167-11T>G	NP_001306145.1:n.1167-11T>G
NM_001319217.2:c.1254-11T>G MANE Select	NP_001306146.1:n.1254-11T>G