Canonical Allele Identifier: CA1245631119
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38080367T= , CM000664.2:g.38080367T= GRCh38
NC_000002.11:g.38307509T= , CM000664.1:g.38307509T= GRCh37
NC_000002.10:g.38161013T= NCBI36
NG_008386.2:g.735A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000494864.1:c.-70-9057A= ENSP00000479876.1:n.-70-9057A=
XM_011533236.1:c.1174+3807T= XP_011531538.1:n.1174+3807T=