Canonical Allele Identifier: CA2658667777

Gene: CYP1B1

Linked Data

• gnomAD v4: 2-38075441-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075441G>T , CM000664.2:g.38075441G>T	GRCh38
NC_000002.11:g.38302584G>T , CM000664.1:g.38302584G>T	GRCh37
NC_000002.10:g.38156088G>T	NCBI36
NG_008386.2:g.5661C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-52C>A	ENSP00000478839.2:n.-1-52C>A
ENST00000610745.5:c.-1-52C>A MANE Select	ENSP00000478561.1:n.-1-52C>A
ENST00000490576.1:c.-1-52C>A	ENSP00000478839.1:n.-1-52C>A
ENST00000494864.1:c.-70-4131C>A	ENSP00000479876.1:n.-70-4131C>A
ENST00000610745.4:c.-1-52C>A	ENSP00000478561.1:n.-1-52C>A
ENST00000613082.1:n.375+339C>A
ENST00000614273.1:c.-1-52C>A	ENSP00000483678.1:n.-1-52C>A
NM_000104.3:c.-1-52C>A	NP_000095.2:n.-1-52C>A
XM_011533236.1:c.55G>T	XP_011531538.1:p.Gly19Trp
NM_000104.4:c.-1-52C>A MANE Select	NP_000095.2:n.-1-52C>A