Canonical Allele Identifier: CA2749545418
Gene: CYP1B1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075466_38075467insACA , CM000664.2:g.38075466_38075467insACA GRCh38
NC_000002.11:g.38302609_38302610insACA , CM000664.1:g.38302609_38302610insACA GRCh37
NC_000002.10:g.38156113_38156114insACA NCBI36
NG_008386.2:g.5635_5636insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-78_-1-77insTGT ENSP00000478839.2:n.-1-78_-1-77insTGT
ENST00000610745.5:c.-1-78_-1-77insTGT MANE Select ENSP00000478561.1:n.-1-78_-1-77insTGT
ENST00000490576.1:c.-1-78_-1-77insTGT ENSP00000478839.1:n.-1-78_-1-77insTGT
ENST00000494864.1:c.-70-4157_-70-4156insTGT ENSP00000479876.1:n.-70-4157_-70-4156insTGT
ENST00000610745.4:c.-1-78_-1-77insTGT ENSP00000478561.1:n.-1-78_-1-77insTGT
ENST00000613082.1:n.375+313_375+314insTGT
ENST00000614273.1:c.-1-78_-1-77insTGT ENSP00000483678.1:n.-1-78_-1-77insTGT
NM_000104.3:c.-1-78_-1-77insTGT NP_000095.2:n.-1-78_-1-77insTGT
XM_011533236.1:c.80_81insACA XP_011531538.1:p.Pro27_Leu28insHis
NM_000104.4:c.-1-78_-1-77insTGT MANE Select NP_000095.2:n.-1-78_-1-77insTGT
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