Canonical Allele Identifier: CA2749544720
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071310_38071311insAGG , CM000664.2:g.38071310_38071311insAGG GRCh38
NC_000002.11:g.38298453_38298454insAGG , CM000664.1:g.38298453_38298454insAGG GRCh37
NC_000002.10:g.38151957_38151958insAGG NCBI36
NG_008386.2:g.9791_9792insCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1044-1_1044insCCT ENSP00000478839.2:n.1044-1_1044insCCT
ENST00000610745.5:c.1044-1_1044insCCT MANE Select ENSP00000478561.1:n.1044-1_1044insCCT
ENST00000492443.1:n.422-1_422insCCT
ENST00000494864.1:c.-70-1_-70insCCT ENSP00000479876.1:n.-70-1_-70insCCT
ENST00000610745.4:c.1044-1_1044insCCT ENSP00000478561.1:n.1044-1_1044insCCT
ENST00000613082.1:n.439-1_439insCCT
ENST00000614273.1:c.1044-1_1044insCCT ENSP00000483678.1:n.1044-1_1044insCCT
NM_000104.3:c.1044-1_1044insCCT NP_000095.2:n.1044-1_1044insCCT
NM_000104.4:c.1044-1_1044insCCT MANE Select NP_000095.2:n.1044-1_1044insCCT