Canonical Allele Identifier: CA1245628425

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075489G= , CM000664.2:g.38075489G=	GRCh38
NC_000002.11:g.38302632G= , CM000664.1:g.38302632G=	GRCh37
NC_000002.10:g.38156136G=	NCBI36
NG_008386.2:g.5613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-100C=	ENSP00000478839.2:n.-1-100C=
ENST00000610745.5:c.-1-100C= MANE Select	ENSP00000478561.1:n.-1-100C=
ENST00000490576.1:c.-1-100C=	ENSP00000478839.1:n.-1-100C=
ENST00000494864.1:c.-70-4179C=	ENSP00000479876.1:n.-70-4179C=
ENST00000610745.4:c.-1-100C=	ENSP00000478561.1:n.-1-100C=
ENST00000613082.1:n.375+291C=
ENST00000614273.1:c.-1-100C=	ENSP00000483678.1:n.-1-100C=
NM_000104.3:c.-1-100C=	NP_000095.2:n.-1-100C=
XM_011533236.1:c.103G=	XP_011531538.1:p.Val35=
NM_000104.4:c.-1-100C= MANE Select	NP_000095.2:n.-1-100C=