Canonical Allele Identifier: CA2658667908

Gene: CYP1B1

Linked Data

• gnomAD v4: 2-38075543-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075543T>G , CM000664.2:g.38075543T>G	GRCh38
NC_000002.11:g.38302686T>G , CM000664.1:g.38302686T>G	GRCh37
NC_000002.10:g.38156190T>G	NCBI36
NG_008386.2:g.5559A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-154A>C	ENSP00000478839.2:n.-1-154A>C
ENST00000610745.5:c.-1-154A>C MANE Select	ENSP00000478561.1:n.-1-154A>C
ENST00000490576.1:c.-1-154A>C	ENSP00000478839.1:n.-1-154A>C
ENST00000494864.1:c.-70-4233A>C	ENSP00000479876.1:n.-70-4233A>C
ENST00000610745.4:c.-1-154A>C	ENSP00000478561.1:n.-1-154A>C
ENST00000613082.1:n.375+237A>C
ENST00000614273.1:c.-1-154A>C	ENSP00000483678.1:n.-1-154A>C
NM_000104.3:c.-1-154A>C	NP_000095.2:n.-1-154A>C
XM_011533236.1:c.157T>G	XP_011531538.1:p.Ser53Ala
NM_000104.4:c.-1-154A>C MANE Select	NP_000095.2:n.-1-154A>C