Canonical Allele Identifier: CA2187827327

Gene: CYP1A2

Linked Data

• dbSNP Id: rs2063333644

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74755366_74755370del , CM000677.2:g.74755366_74755370del	GRCh38
NC_000015.9:g.75047707_75047711del , CM000677.1:g.75047707_75047711del	GRCh37
NC_000015.8:g.72834760_72834764del	NCBI36
NG_008431.1:g.37825_37829del
NG_008431.2:g.37825_37829del
NG_061543.1:g.11522_11526del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343932.5:c.*278_*282del MANE Select	ENSP00000342007.4:n.*278_*282del
ENST00000343932.4:c.*278_*282del	ENSP00000342007.4:n.*278_*282del
NM_000761.4:c.*278_*282del	NP_000752.2:n.*278_*282del
NM_000761.5:c.*278_*282del MANE Select	NP_000752.2:n.*278_*282del