Canonical Allele Identifier: CA1245628768
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076192T= , CM000664.2:g.38076192T= GRCh38
NC_000002.11:g.38303334T= , CM000664.1:g.38303334T= GRCh37
NC_000002.10:g.38156838T= NCBI36
NG_008386.2:g.4910A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-175A= ENSP00000478839.2:n.-175A=
ENST00000494864.1:c.-70-4882A= ENSP00000479876.1:n.-70-4882A=
XM_011533236.1:c.806T= XP_011531538.1:p.Val269=