Canonical Allele Identifier: CA1245628770
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076193A= , CM000664.2:g.38076193A= GRCh38
NC_000002.11:g.38303335A= , CM000664.1:g.38303335A= GRCh37
NC_000002.10:g.38156839A= NCBI36
NG_008386.2:g.4909T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-176T= ENSP00000478839.2:n.-176T=
ENST00000494864.1:c.-70-4883T= ENSP00000479876.1:n.-70-4883T=
XM_011533236.1:c.807A= XP_011531538.1:p.Val269=