Canonical Allele Identifier: CA1245628480
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075591C= , CM000664.2:g.38075591C= GRCh38
NC_000002.11:g.38302734C= , CM000664.1:g.38302734C= GRCh37
NC_000002.10:g.38156238C= NCBI36
NG_008386.2:g.5511G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-202G= ENSP00000478839.2:n.-1-202G=
ENST00000610745.5:c.-2+189G= MANE Select ENSP00000478561.1:n.-2+189G=
ENST00000490576.1:c.-1-202G= ENSP00000478839.1:n.-1-202G=
ENST00000494864.1:c.-70-4281G= ENSP00000479876.1:n.-70-4281G=
ENST00000610745.4:c.-2+189G= ENSP00000478561.1:n.-2+189G=
ENST00000613082.1:n.375+189G=
ENST00000614273.1:c.-2+185G= ENSP00000483678.1:n.-2+185G=
NM_000104.3:c.-2+189G= NP_000095.2:n.-2+189G=
XM_011533236.1:c.205C= XP_011531538.1:p.Arg69=
NM_000104.4:c.-2+189G= MANE Select NP_000095.2:n.-2+189G=
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