Canonical Allele Identifier: CA1245625056

Gene: CYP1B1 RMDN2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38068790A= , CM000664.2:g.38068790A=	GRCh38
NC_000002.11:g.38295933A= , CM000664.1:g.38295933A=	GRCh37
NC_000002.10:g.38149437A=	NCBI36
NG_008386.2:g.12312T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000490576.2:c.*1932T= (CYP1B1)	ENSP00000478839.2:n.*1932T=
ENST00000610745.5:c.*1932T= (CYP1B1) MANE Select	ENSP00000478561.1:n.*1932T=
ENST00000491456.1:n.184+388T= (CYP1B1)
ENST00000610745.4:c.*1932T= (CYP1B1)	ENSP00000478561.1:n.*1932T=
NM_000104.3:c.*1932T= (CYP1B1)	NP_000095.2:n.*1932T=
XR_939668.1:n.3790A= (RMDN2)
XM_011532615.3:c.*1836A= (RMDN2)	XP_011530917.2:n.*1836A=
XM_017003475.2:c.*1800A= (RMDN2)	XP_016858964.1:n.*1800A=
XR_939668.3:n.3921A= (RMDN2)
NM_000104.4:c.*1932T= (CYP1B1) MANE Select	NP_000095.2:n.*1932T=