Canonical Allele Identifier: CA1245628479

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075587A= , CM000664.2:g.38075587A=	GRCh38
NC_000002.11:g.38302730A= , CM000664.1:g.38302730A=	GRCh37
NC_000002.10:g.38156234A=	NCBI36
NG_008386.2:g.5515T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-198T=	ENSP00000478839.2:n.-1-198T=
ENST00000610745.5:c.-2+193T= MANE Select	ENSP00000478561.1:n.-2+193T=
ENST00000490576.1:c.-1-198T=	ENSP00000478839.1:n.-1-198T=
ENST00000494864.1:c.-70-4277T=	ENSP00000479876.1:n.-70-4277T=
ENST00000610745.4:c.-2+193T=	ENSP00000478561.1:n.-2+193T=
ENST00000613082.1:n.375+193T=
ENST00000614273.1:c.-2+189T=	ENSP00000483678.1:n.-2+189T=
NM_000104.3:c.-2+193T=	NP_000095.2:n.-2+193T=
XM_011533236.1:c.201A=	XP_011531538.1:p.Pro67=
NM_000104.4:c.-2+193T= MANE Select	NP_000095.2:n.-2+193T=