Canonical Allele Identifier: CA272812526

Gene: CYP1A1

Linked Data

• dbSNP Id: rs973613520
• gnomAD v2: 15-75011968-C-A
• gnomAD v3: 15-74719627-C-A
• gnomAD v4: 15-74719627-C-A
• MyVariant Identifiers: chr15:g.75011968C>A (hg19) ; chr15:g.74719627C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719627C>A , CM000677.2:g.74719627C>A	GRCh38
NC_000015.9:g.75011968C>A , CM000677.1:g.75011968C>A	GRCh37
NC_000015.8:g.72799021C>A	NCBI36
NG_008431.1:g.2086C>A
NG_008431.2:g.2086C>A
NG_061374.1:g.10902G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*862G>T MANE Select	ENSP00000369050.3:n.*862G>T
ENST00000379727.7:c.*862G>T	ENSP00000369050.3:n.*862G>T
ENST00000395048.6:c.*862G>T	ENSP00000378488.2:n.*862G>T
ENST00000612821.4:c.2317G>T	ENSP00000479744.1:n.2317G>T
ENST00000617691.4:c.*862G>T	ENSP00000482863.1:n.*862G>T
NM_000499.3:c.*862G>T	NP_000490.1:n.*862G>T
XM_005254185.1:c.*862G>T	XP_005254242.1:n.*862G>T
NM_000499.5:c.*862G>T	NP_000490.1:n.*862G>T
NM_001319216.2:c.*862G>T	NP_001306145.1:n.*862G>T
NM_001319217.2:c.*862G>T MANE Select	NP_001306146.1:n.*862G>T