Canonical Allele Identifier: CA1245628431
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075495A= , CM000664.2:g.38075495A= GRCh38
NC_000002.11:g.38302638A= , CM000664.1:g.38302638A= GRCh37
NC_000002.10:g.38156142A= NCBI36
NG_008386.2:g.5607T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-106T= ENSP00000478839.2:n.-1-106T=
ENST00000610745.5:c.-1-106T= MANE Select ENSP00000478561.1:n.-1-106T=
ENST00000490576.1:c.-1-106T= ENSP00000478839.1:n.-1-106T=
ENST00000494864.1:c.-70-4185T= ENSP00000479876.1:n.-70-4185T=
ENST00000610745.4:c.-1-106T= ENSP00000478561.1:n.-1-106T=
ENST00000613082.1:n.375+285T=
ENST00000614273.1:c.-1-106T= ENSP00000483678.1:n.-1-106T=
NM_000104.3:c.-1-106T= NP_000095.2:n.-1-106T=
XM_011533236.1:c.109A= XP_011531538.1:p.Arg37=
NM_000104.4:c.-1-106T= MANE Select NP_000095.2:n.-1-106T=
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