Canonical Allele Identifier: CA619412553

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1300786635
• gnomAD v2: 15-75013154-G-T
• gnomAD v4: 15-74720813-G-T
• MyVariant Identifiers: chr15:g.75013154G>T (hg19) ; chr15:g.74720813G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720813G>T , CM000677.2:g.74720813G>T	GRCh38
NC_000015.9:g.75013154G>T , CM000677.1:g.75013154G>T	GRCh37
NC_000015.8:g.72800207G>T	NCBI36
NG_008431.1:g.3272G>T
NG_008431.2:g.3272G>T
NG_061374.1:g.9716C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1254-39C>A MANE Select	ENSP00000369050.3:n.1254-39C>A
ENST00000379727.7:c.1254-39C>A	ENSP00000369050.3:n.1254-39C>A
ENST00000395048.6:c.1254-39C>A	ENSP00000378488.2:n.1254-39C>A
ENST00000395049.8:c.1167-39C>A	ENSP00000378489.4:n.1167-39C>A
ENST00000562201.5:c.*491-39C>A	ENSP00000455340.1:n.*491-39C>A
ENST00000564596.5:c.*150C>A	ENSP00000457668.1:n.*150C>A
ENST00000566503.1:c.471-39C>A	ENSP00000455846.1:n.471-39C>A
ENST00000567032.5:c.1254-39C>A	ENSP00000456585.1:n.1254-39C>A
ENST00000569630.5:c.*843-39C>A	ENSP00000455051.1:n.*843-39C>A
ENST00000612821.4:c.1170-39C>A	ENSP00000479744.1:n.1170-39C>A
ENST00000617691.4:c.1167-39C>A	ENSP00000482863.1:n.1167-39C>A
NM_000499.3:c.1254-39C>A	NP_000490.1:n.1254-39C>A
XM_005254185.1:c.1254-39C>A	XP_005254242.1:n.1254-39C>A
NM_000499.5:c.1254-39C>A	NP_000490.1:n.1254-39C>A
NM_001319216.2:c.1167-39C>A	NP_001306145.1:n.1167-39C>A
NM_001319217.2:c.1254-39C>A MANE Select	NP_001306146.1:n.1254-39C>A