Canonical Allele Identifier: CA1245628485

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075600C= , CM000664.2:g.38075600C=	GRCh38
NC_000002.11:g.38302743C= , CM000664.1:g.38302743C=	GRCh37
NC_000002.10:g.38156247C=	NCBI36
NG_008386.2:g.5502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-211G=	ENSP00000478839.2:n.-1-211G=
ENST00000610745.5:c.-2+180G= MANE Select	ENSP00000478561.1:n.-2+180G=
ENST00000490576.1:c.-1-211G=	ENSP00000478839.1:n.-1-211G=
ENST00000494864.1:c.-70-4290G=	ENSP00000479876.1:n.-70-4290G=
ENST00000610745.4:c.-2+180G=	ENSP00000478561.1:n.-2+180G=
ENST00000613082.1:n.375+180G=
ENST00000614273.1:c.-2+176G=	ENSP00000483678.1:n.-2+176G=
NM_000104.3:c.-2+180G=	NP_000095.2:n.-2+180G=
XM_011533236.1:c.214C=	XP_011531538.1:p.Pro72=
NM_000104.4:c.-2+180G= MANE Select	NP_000095.2:n.-2+180G=