Canonical Allele Identifier: CA2187827319

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063333608
• gnomAD v3: 15-74755363-A-AAC
• gnomAD v4: 15-74755363-A-AAC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755364_74755365insCA , CM000677.2:g.74755364_74755365insCA	GRCh38
NC_000015.9:g.75047705_75047706insCA , CM000677.1:g.75047705_75047706insCA	GRCh37
NC_000015.8:g.72834758_72834759insCA	NCBI36
NG_008431.1:g.37823_37824insCA
NG_008431.2:g.37823_37824insCA
NG_061543.1:g.11520_11521insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*276_*277insCA MANE Select	ENSP00000342007.4:n.*276_*277insCA
ENST00000343932.4:c.*276_*277insCA	ENSP00000342007.4:n.*276_*277insCA
NM_000761.4:c.*276_*277insCA	NP_000752.2:n.*276_*277insCA
NM_000761.5:c.*276_*277insCA MANE Select	NP_000752.2:n.*276_*277insCA