Canonical Allele Identifier: CA1245628382

Gene: CYP1B1

Linked Data

• dbSNP Id: rs1682520315

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075417A>G , CM000664.2:g.38075417A>G	GRCh38
NC_000002.11:g.38302560A>G , CM000664.1:g.38302560A>G	GRCh37
NC_000002.10:g.38156064A>G	NCBI36
NG_008386.2:g.5685T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-28T>C	ENSP00000478839.2:n.-1-28T>C
ENST00000610745.5:c.-1-28T>C MANE Select	ENSP00000478561.1:n.-1-28T>C
ENST00000490576.1:c.-1-28T>C	ENSP00000478839.1:n.-1-28T>C
ENST00000494864.1:c.-70-4107T>C	ENSP00000479876.1:n.-70-4107T>C
ENST00000610745.4:c.-1-28T>C	ENSP00000478561.1:n.-1-28T>C
ENST00000613082.1:n.375+363T>C
ENST00000614273.1:c.-1-28T>C	ENSP00000483678.1:n.-1-28T>C
NM_000104.3:c.-1-28T>C	NP_000095.2:n.-1-28T>C
XM_011533236.1:c.31A>G	XP_011531538.1:p.Thr11Ala
NM_000104.4:c.-1-28T>C MANE Select	NP_000095.2:n.-1-28T>C