Canonical Allele Identifier: CA1245626048
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38070972A= , CM000664.2:g.38070972A= GRCh38
NC_000002.11:g.38298115A= , CM000664.1:g.38298115A= GRCh37
NC_000002.10:g.38151619A= NCBI36
NG_008386.2:g.10130T=

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.1382T= ENSP00000478839.2:p.Met461=
ENST00000610745.5:c.1382T= MANE Select ENSP00000478561.1:p.Met461=
ENST00000494864.1:c.269T= ENSP00000479876.1:p.Met90=
ENST00000610745.4:c.1382T= ENSP00000478561.1:p.Met461=
ENST00000614273.1:c.1382T= ENSP00000483678.1:p.Met461=
NM_000104.3:c.1382T= NP_000095.2:p.Met461=
NM_000104.4:c.1382T= MANE Select NP_000095.2:p.Met461=