Canonical Allele Identifier: CA1245628094
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38074980A= , CM000664.2:g.38074980A= GRCh38
NC_000002.11:g.38302123A= , CM000664.1:g.38302123A= GRCh37
NC_000002.10:g.38155627A= NCBI36
NG_008386.2:g.6122T=

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.409T= ENSP00000478839.2:p.Tyr137=
ENST00000610745.5:c.409T= MANE Select ENSP00000478561.1:p.Tyr137=
ENST00000490576.1:c.409T= ENSP00000478839.1:p.Tyr137=
ENST00000494864.1:c.-70-3670T= ENSP00000479876.1:n.-70-3670T=
ENST00000610745.4:c.409T= ENSP00000478561.1:p.Tyr137=
ENST00000613082.1:n.376-572T=
ENST00000614273.1:c.409T= ENSP00000483678.1:p.Tyr137=
NM_000104.3:c.409T= NP_000095.2:p.Tyr137=
NM_000104.4:c.409T= MANE Select NP_000095.2:p.Tyr137=