Canonical Allele Identifier: CA2749546734
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075545_38075546insAGT , CM000664.2:g.38075545_38075546insAGT GRCh38
NC_000002.11:g.38302688_38302689insAGT , CM000664.1:g.38302688_38302689insAGT GRCh37
NC_000002.10:g.38156192_38156193insAGT NCBI36
NG_008386.2:g.5556_5557insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-157_-1-156insACT ENSP00000478839.2:n.-1-157_-1-156insACT
ENST00000610745.5:c.-1-157_-1-156insACT MANE Select ENSP00000478561.1:n.-1-157_-1-156insACT
ENST00000490576.1:c.-1-157_-1-156insACT ENSP00000478839.1:n.-1-157_-1-156insACT
ENST00000494864.1:c.-70-4236_-70-4235insACT ENSP00000479876.1:n.-70-4236_-70-4235insACT
ENST00000610745.4:c.-1-157_-1-156insACT ENSP00000478561.1:n.-1-157_-1-156insACT
ENST00000613082.1:n.375+234_375+235insACT
ENST00000614273.1:c.-1-157_-1-156insACT ENSP00000483678.1:n.-1-157_-1-156insACT
NM_000104.3:c.-1-157_-1-156insACT NP_000095.2:n.-1-157_-1-156insACT
XM_011533236.1:c.159_160insAGT XP_011531538.1:p.Ser53_Pro54insSer
NM_000104.4:c.-1-157_-1-156insACT MANE Select NP_000095.2:n.-1-157_-1-156insACT
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