Canonical Allele Identifier: CA1245628775
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38076200G= , CM000664.2:g.38076200G= GRCh38
NC_000002.11:g.38303342G= , CM000664.1:g.38303342G= GRCh37
NC_000002.10:g.38156846G= NCBI36
NG_008386.2:g.4902C=

Transcript Alleles

HGVS Amino-acid change
ENST00000494864.1:c.-70-4890C= ENSP00000479876.1:n.-70-4890C=
XM_011533236.1:c.814G= XP_011531538.1:p.Gly272=