Canonical Allele Identifier: CA3006920437

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075156_38075157del , CM000664.2:g.38075156_38075157del	GRCh38
NC_000002.11:g.38302299_38302300del , CM000664.1:g.38302299_38302300del	GRCh37
NC_000002.10:g.38155803_38155804del	NCBI36
NG_008386.2:g.5948_5949del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.235_236del	ENSP00000478839.2:p.Arg79AlafsTer?
ENST00000610745.5:c.235_236del MANE Select	ENSP00000478561.1:p.Arg79AlafsTer?
ENST00000490576.1:c.235_236del	ENSP00000478839.1:p.Arg79AlafsTer?
ENST00000494864.1:c.-70-3844_-70-3843del	ENSP00000479876.1:n.-70-3844_-70-3843del
ENST00000610745.4:c.235_236del	ENSP00000478561.1:p.Arg79AlafsTer?
ENST00000613082.1:n.375+626_375+627del
ENST00000614273.1:c.235_236del	ENSP00000483678.1:p.Arg79AlafsTer?
NM_000104.3:c.235_236del	NP_000095.2:p.Arg79AlafsTer?
NM_000104.4:c.235_236del MANE Select	NP_000095.2:p.Arg79AlafsTer?