Canonical Allele Identifier: CA2749545407
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075410_38075569del , CM000664.2:g.38075410_38075569del GRCh38
NC_000002.11:g.38302553_38302712del , CM000664.1:g.38302553_38302712del GRCh37
NC_000002.10:g.38156057_38156216del NCBI36
NG_008386.2:g.5540_5699del

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-173_-1-14del ENSP00000478839.2:n.-1-173_-1-14del
ENST00000610745.5:c.-1-173_-1-14del MANE Select ENSP00000478561.1:n.-1-173_-1-14del
ENST00000490576.1:c.-1-173_-1-14del ENSP00000478839.1:n.-1-173_-1-14del
ENST00000494864.1:c.-70-4252_-70-4093del ENSP00000479876.1:n.-70-4252_-70-4093del
ENST00000610745.4:c.-1-173_-1-14del ENSP00000478561.1:n.-1-173_-1-14del
ENST00000613082.1:n.375+218_375+377del
ENST00000614273.1:c.-1-173_-1-14del ENSP00000483678.1:n.-1-173_-1-14del
NM_000104.3:c.-1-173_-1-14del NP_000095.2:n.-1-173_-1-14del
XM_011533236.1:c.24_183del XP_011531538.1:p.Arg9GlufsTer?
NM_000104.4:c.-1-173_-1-14del MANE Select NP_000095.2:n.-1-173_-1-14del