Canonical Allele Identifier: CA272812527

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1034900746
• gnomAD v2: 15-75011973-A-C
• gnomAD v3: 15-74719632-A-C
• gnomAD v4: 15-74719632-A-C
• MyVariant Identifiers: chr15:g.75011973A>C (hg19) ; chr15:g.74719632A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719632A>C , CM000677.2:g.74719632A>C	GRCh38
NC_000015.9:g.75011973A>C , CM000677.1:g.75011973A>C	GRCh37
NC_000015.8:g.72799026A>C	NCBI36
NG_008431.1:g.2091A>C
NG_008431.2:g.2091A>C
NG_061374.1:g.10897T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*857T>G MANE Select	ENSP00000369050.3:n.*857T>G
ENST00000379727.7:c.*857T>G	ENSP00000369050.3:n.*857T>G
ENST00000395048.6:c.*857T>G	ENSP00000378488.2:n.*857T>G
ENST00000612821.4:c.2312T>G	ENSP00000479744.1:n.2312T>G
ENST00000617691.4:c.*857T>G	ENSP00000482863.1:n.*857T>G
NM_000499.3:c.*857T>G	NP_000490.1:n.*857T>G
XM_005254185.1:c.*857T>G	XP_005254242.1:n.*857T>G
NM_000499.5:c.*857T>G	NP_000490.1:n.*857T>G
NM_001319216.2:c.*857T>G	NP_001306145.1:n.*857T>G
NM_001319217.2:c.*857T>G MANE Select	NP_001306146.1:n.*857T>G