Canonical Allele Identifier: CA7659254

Gene: CYP1A1

Linked Data

• dbSNP Id: rs760050326
• ExAC: 15:75013024 T / A
• gnomAD v2: 15-75013024-T-A
• gnomAD v4: 15-74720683-T-A
• MyVariant Identifiers: chr15:g.75013024T>A (hg19) ; chr15:g.74720683T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720683T>A , CM000677.2:g.74720683T>A	GRCh38
NC_000015.9:g.75013024T>A , CM000677.1:g.75013024T>A	GRCh37
NC_000015.8:g.72800077T>A	NCBI36
NG_008431.1:g.3142T>A
NG_008431.2:g.3142T>A
NG_061374.1:g.9846A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1345A>T MANE Select	ENSP00000369050.3:p.Ile449Phe
ENST00000379727.7:c.1345A>T	ENSP00000369050.3:p.Ile449Phe
ENST00000395048.6:c.1345A>T	ENSP00000378488.2:p.Ile449Phe
ENST00000395049.8:c.1258A>T	ENSP00000378489.4:p.Ile420Phe
ENST00000567032.5:c.1345A>T	ENSP00000456585.1:p.Ile449Phe
ENST00000612821.4:c.1261A>T	ENSP00000479744.1:p.Ile421Phe
ENST00000617691.4:c.1258A>T	ENSP00000482863.1:p.Ile420Phe
NM_000499.3:c.1345A>T	NP_000490.1:p.Ile449Phe
XM_005254185.1:c.1345A>T	XP_005254242.1:p.Ile449Phe
NM_000499.5:c.1345A>T	NP_000490.1:p.Ile449Phe
NM_001319216.2:c.1258A>T	NP_001306145.1:p.Ile420Phe
NM_001319217.2:c.1345A>T MANE Select	NP_001306146.1:p.Ile449Phe