Canonical Allele Identifier: CA7660149

Gene: CYP1A2

Linked Data

• dbSNP Id: rs752887393
• ExAC: 15:75047439 C / A
• gnomAD v2: 15-75047439-C-A
• gnomAD v3: 15-74755098-C-A
• gnomAD v4: 15-74755098-C-A
• MyVariant Identifiers: chr15:g.75047439C>A (hg19) ; chr15:g.74755098C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755098C>A , CM000677.2:g.74755098C>A	GRCh38
NC_000015.9:g.75047439C>A , CM000677.1:g.75047439C>A	GRCh37
NC_000015.8:g.72834492C>A	NCBI36
NG_008431.1:g.37557C>A
NG_008431.2:g.37557C>A
NG_061543.1:g.11254C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*10C>A MANE Select	ENSP00000342007.4:n.*10C>A
ENST00000343932.4:c.*10C>A	ENSP00000342007.4:n.*10C>A
NM_000761.4:c.*10C>A	NP_000752.2:n.*10C>A
NM_000761.5:c.*10C>A MANE Select	NP_000752.2:n.*10C>A