Canonical Allele Identifier: CA7660148

Gene: CYP1A2

Linked Data

• dbSNP Id: rs765216472
• ExAC: 15:75047437 A / C
• gnomAD v2: 15-75047437-A-C
• gnomAD v3: 15-74755096-A-C
• gnomAD v4: 15-74755096-A-C
• MyVariant Identifiers: chr15:g.75047437A>C (hg19) ; chr15:g.74755096A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755096A>C , CM000677.2:g.74755096A>C	GRCh38
NC_000015.9:g.75047437A>C , CM000677.1:g.75047437A>C	GRCh37
NC_000015.8:g.72834490A>C	NCBI36
NG_008431.1:g.37555A>C
NG_008431.2:g.37555A>C
NG_061543.1:g.11252A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*8A>C MANE Select	ENSP00000342007.4:n.*8A>C
ENST00000343932.4:c.*8A>C	ENSP00000342007.4:n.*8A>C
NM_000761.4:c.*8A>C	NP_000752.2:n.*8A>C
NM_000761.5:c.*8A>C MANE Select	NP_000752.2:n.*8A>C