Canonical Allele Identifier: CA7660118

Gene: CYP1A2

Linked Data

• dbSNP Id: rs761121295
• ExAC: 15:75047333 G / A
• gnomAD v2: 15-75047333-G-A
• gnomAD v3: 15-74754992-G-A
• gnomAD v4: 15-74754992-G-A
• COSMIC: COSM701190
• MyVariant Identifiers: chr15:g.75047333G>A (hg19) ; chr15:g.74754992G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74754992G>A , CM000677.2:g.74754992G>A	GRCh38
NC_000015.9:g.75047333G>A , CM000677.1:g.75047333G>A	GRCh37
NC_000015.8:g.72834386G>A	NCBI36
NG_008431.1:g.37451G>A
NG_008431.2:g.37451G>A
NG_061543.1:g.11148G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.1455G>A MANE Select	ENSP00000342007.4:p.Pro485=
ENST00000343932.4:c.1455G>A	ENSP00000342007.4:p.Pro485=
NM_000761.4:c.1455G>A	NP_000752.2:p.Pro485=
NM_000761.5:c.1455G>A MANE Select	NP_000752.2:p.Pro485=