Canonical Allele Identifier: CA1245628271
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075242G= , CM000664.2:g.38075242G= GRCh38
NC_000002.11:g.38302385G= , CM000664.1:g.38302385G= GRCh37
NC_000002.10:g.38155889G= NCBI36
NG_008386.2:g.5860C=

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.147C= ENSP00000478839.2:p.Ser49=
ENST00000610745.5:c.147C= MANE Select ENSP00000478561.1:p.Ser49=
ENST00000490576.1:c.147C= ENSP00000478839.1:p.Ser49=
ENST00000494864.1:c.-70-3932C= ENSP00000479876.1:n.-70-3932C=
ENST00000610745.4:c.147C= ENSP00000478561.1:p.Ser49=
ENST00000613082.1:n.375+538C=
ENST00000614273.1:c.147C= ENSP00000483678.1:p.Ser49=
NM_000104.3:c.147C= NP_000095.2:p.Ser49=
NM_000104.4:c.147C= MANE Select NP_000095.2:p.Ser49=