Canonical Allele Identifier: CA346329662
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075159A>C , CM000664.2:g.38075159A>C GRCh38
NC_000002.11:g.38302302A>C , CM000664.1:g.38302302A>C GRCh37
NC_000002.10:g.38155806A>C NCBI36
NG_008386.2:g.5943T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.230T>G ENSP00000478839.2:p.Leu77Arg
ENST00000610745.5:c.230T>G MANE Select ENSP00000478561.1:p.Leu77Arg
ENST00000490576.1:c.230T>G ENSP00000478839.1:p.Leu77Arg
ENST00000494864.1:c.-70-3849T>G ENSP00000479876.1:n.-70-3849T>G
ENST00000610745.4:c.230T>G ENSP00000478561.1:p.Leu77Arg
ENST00000613082.1:n.375+621T>G
ENST00000614273.1:c.230T>G ENSP00000483678.1:p.Leu77Arg
NM_000104.3:c.230T>G NP_000095.2:p.Leu77Arg
NM_000104.4:c.230T>G MANE Select NP_000095.2:p.Leu77Arg