Canonical Allele Identifier: CA491488342

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063161751
• gnomAD v4: 15-74720726-G-A
• MyVariant Identifiers: chr15:g.75013067G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720726G>A , CM000677.2:g.74720726G>A	GRCh38
NC_000015.9:g.75013067G>A , CM000677.1:g.75013067G>A	GRCh37
NC_000015.8:g.72800120G>A	NCBI36
NG_008431.1:g.3185G>A
NG_008431.2:g.3185G>A
NG_061374.1:g.9803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1302C>T MANE Select	ENSP00000369050.3:p.Thr434=
ENST00000379727.7:c.1302C>T	ENSP00000369050.3:p.Thr434=
ENST00000395048.6:c.1302C>T	ENSP00000378488.2:p.Thr434=
ENST00000395049.8:c.1215C>T	ENSP00000378489.4:p.Thr405=
ENST00000562201.5:c.*539C>T	ENSP00000455340.1:n.*539C>T
ENST00000564596.5:c.*237C>T	ENSP00000457668.1:n.*237C>T
ENST00000566503.1:c.519C>T	ENSP00000455846.1:p.Thr173=
ENST00000567032.5:c.1302C>T	ENSP00000456585.1:p.Thr434=
ENST00000569630.5:c.*891C>T	ENSP00000455051.1:n.*891C>T
ENST00000612821.4:c.1218C>T	ENSP00000479744.1:p.Thr406=
ENST00000617691.4:c.1215C>T	ENSP00000482863.1:p.Thr405=
NM_000499.3:c.1302C>T	NP_000490.1:p.Thr434=
XM_005254185.1:c.1302C>T	XP_005254242.1:p.Thr434=
NM_000499.5:c.1302C>T	NP_000490.1:p.Thr434=
NM_001319216.2:c.1215C>T	NP_001306145.1:p.Thr405=
NM_001319217.2:c.1302C>T MANE Select	NP_001306146.1:p.Thr434=