Canonical Allele Identifier: CA2749544725
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071314T>C , CM000664.2:g.38071314T>C GRCh38
NC_000002.11:g.38298457T>C , CM000664.1:g.38298457T>C GRCh37
NC_000002.10:g.38151961T>C NCBI36
NG_008386.2:g.9788A>G

Transcript Alleles

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