Canonical Allele Identifier: CA1245625051

Gene: CYP1B1 RMDN2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38068777T= , CM000664.2:g.38068777T=	GRCh38
NC_000002.11:g.38295920T= , CM000664.1:g.38295920T=	GRCh37
NC_000002.10:g.38149424T=	NCBI36
NG_008386.2:g.12325A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000490576.2:c.*1945A= (CYP1B1)	ENSP00000478839.2:n.*1945A=
ENST00000610745.5:c.*1945A= (CYP1B1) MANE Select	ENSP00000478561.1:n.*1945A=
ENST00000491456.1:n.184+401A= (CYP1B1)
ENST00000610745.4:c.*1945A= (CYP1B1)	ENSP00000478561.1:n.*1945A=
NM_000104.3:c.*1945A= (CYP1B1)	NP_000095.2:n.*1945A=
XR_939668.1:n.3777T= (RMDN2)
XM_011532615.3:c.*1823T= (RMDN2)	XP_011530917.2:n.*1823T=
XM_017003475.2:c.*1787T= (RMDN2)	XP_016858964.1:n.*1787T=
XR_939668.3:n.3908T= (RMDN2)
NM_000104.4:c.*1945A= (CYP1B1) MANE Select	NP_000095.2:n.*1945A=