Canonical Allele Identifier: CA2658667990

Gene: CYP1B1

Linked Data

• gnomAD v4: 2-38075591-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075591C>T , CM000664.2:g.38075591C>T	GRCh38
NC_000002.11:g.38302734C>T , CM000664.1:g.38302734C>T	GRCh37
NC_000002.10:g.38156238C>T	NCBI36
NG_008386.2:g.5511G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-202G>A	ENSP00000478839.2:n.-1-202G>A
ENST00000610745.5:c.-2+189G>A MANE Select	ENSP00000478561.1:n.-2+189G>A
ENST00000490576.1:c.-1-202G>A	ENSP00000478839.1:n.-1-202G>A
ENST00000494864.1:c.-70-4281G>A	ENSP00000479876.1:n.-70-4281G>A
ENST00000610745.4:c.-2+189G>A	ENSP00000478561.1:n.-2+189G>A
ENST00000613082.1:n.375+189G>A
ENST00000614273.1:c.-2+185G>A	ENSP00000483678.1:n.-2+185G>A
NM_000104.3:c.-2+189G>A	NP_000095.2:n.-2+189G>A
XM_011533236.1:c.205C>T	XP_011531538.1:p.Arg69Cys
NM_000104.4:c.-2+189G>A MANE Select	NP_000095.2:n.-2+189G>A