Canonical Allele Identifier: CA2749545433
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075502dup , CM000664.2:g.38075502dup GRCh38
NC_000002.11:g.38302645dup , CM000664.1:g.38302645dup GRCh37
NC_000002.10:g.38156149dup NCBI36
NG_008386.2:g.5600dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-113dup ENSP00000478839.2:n.-1-113dup
ENST00000610745.5:c.-1-113dup MANE Select ENSP00000478561.1:n.-1-113dup
ENST00000490576.1:c.-1-113dup ENSP00000478839.1:n.-1-113dup
ENST00000494864.1:c.-70-4192dup ENSP00000479876.1:n.-70-4192dup
ENST00000610745.4:c.-1-113dup ENSP00000478561.1:n.-1-113dup
ENST00000613082.1:n.375+278dup
ENST00000614273.1:c.-1-113dup ENSP00000483678.1:n.-1-113dup
NM_000104.3:c.-1-113dup NP_000095.2:n.-1-113dup
XM_011533236.1:c.116dup XP_011531538.1:p.Leu40AlafsTer?
NM_000104.4:c.-1-113dup MANE Select NP_000095.2:n.-1-113dup