Canonical Allele Identifier: CA1245628086
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38074965T= , CM000664.2:g.38074965T= GRCh38
NC_000002.11:g.38302108T= , CM000664.1:g.38302108T= GRCh37
NC_000002.10:g.38155612T= NCBI36
NG_008386.2:g.6137A=

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.424A= ENSP00000478839.2:p.Lys142=
ENST00000610745.5:c.424A= MANE Select ENSP00000478561.1:p.Lys142=
ENST00000490576.1:c.424A= ENSP00000478839.1:p.Lys142=
ENST00000494864.1:c.-70-3655A= ENSP00000479876.1:n.-70-3655A=
ENST00000610745.4:c.424A= ENSP00000478561.1:p.Lys142=
ENST00000613082.1:n.376-557A=
ENST00000614273.1:c.424A= ENSP00000483678.1:p.Lys142=
NM_000104.3:c.424A= NP_000095.2:p.Lys142=
NM_000104.4:c.424A= MANE Select NP_000095.2:p.Lys142=