Canonical Allele Identifier: CA7660160

Gene: CYP1A2

Linked Data

• dbSNP Id: rs747668209
• ExAC: 15:75047469 G / GC
• gnomAD v2: 15-75047469-G-GC
• MyVariant Identifiers: chr15:g.75047469_75047470insC (hg19) ; chr15:g.74755128_74755129insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755130dup , CM000677.2:g.74755130dup	GRCh38
NC_000015.9:g.75047471dup , CM000677.1:g.75047471dup	GRCh37
NC_000015.8:g.72834524dup	NCBI36
NG_008431.1:g.37589dup
NG_008431.2:g.37589dup
NG_061543.1:g.11286dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*42dup MANE Select	ENSP00000342007.4:n.*42dup
ENST00000343932.4:c.*42dup	ENSP00000342007.4:n.*42dup
NM_000761.4:c.*42dup	NP_000752.2:n.*42dup
NM_000761.5:c.*42dup MANE Select	NP_000752.2:n.*42dup