Canonical Allele Identifier: CA7659774

Gene: CYP1A2

Linked Data

• dbSNP Id: rs752542857
• ExAC: 15:75042487 C / A
• gnomAD v2: 15-75042487-C-A
• gnomAD v3: 15-74750146-C-A
• gnomAD v4: 15-74750146-C-A
• MyVariant Identifiers: chr15:g.75042487C>A (hg19) ; chr15:g.74750146C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74750146C>A , CM000677.2:g.74750146C>A	GRCh38
NC_000015.9:g.75042487C>A , CM000677.1:g.75042487C>A	GRCh37
NC_000015.8:g.72829540C>A	NCBI36
NG_008431.1:g.32605C>A
NG_008431.2:g.32605C>A
NG_061543.1:g.6302C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.408C>A MANE Select	ENSP00000342007.4:p.Arg136=
ENST00000343932.4:c.408C>A	ENSP00000342007.4:p.Arg136=
NM_000761.4:c.408C>A	NP_000752.2:p.Arg136=
NM_000761.5:c.408C>A MANE Select	NP_000752.2:p.Arg136=