Canonical Allele Identifier: CA2187827297

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063333380
• gnomAD v4: 15-74755349-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755349_74755350insA , CM000677.2:g.74755349_74755350insA	GRCh38
NC_000015.9:g.75047690_75047691insA , CM000677.1:g.75047690_75047691insA	GRCh37
NC_000015.8:g.72834743_72834744insA	NCBI36
NG_008431.1:g.37808_37809insA
NG_008431.2:g.37808_37809insA
NG_061543.1:g.11505_11506insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*261_*262insA MANE Select	ENSP00000342007.4:n.*261_*262insA
ENST00000343932.4:c.*261_*262insA	ENSP00000342007.4:n.*261_*262insA
NM_000761.4:c.*261_*262insA	NP_000752.2:n.*261_*262insA
NM_000761.5:c.*261_*262insA MANE Select	NP_000752.2:n.*261_*262insA