Canonical Allele Identifier: CA346327941
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071296T>C , CM000664.2:g.38071296T>C GRCh38
NC_000002.11:g.38298439T>C , CM000664.1:g.38298439T>C GRCh37
NC_000002.10:g.38151943T>C NCBI36
NG_008386.2:g.9806A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1058A>G ENSP00000478839.2:p.Gln353Arg
ENST00000610745.5:c.1058A>G MANE Select ENSP00000478561.1:p.Gln353Arg
ENST00000492443.1:n.436A>G
ENST00000494864.1:c.-56A>G ENSP00000479876.1:n.-56A>G
ENST00000610745.4:c.1058A>G ENSP00000478561.1:p.Gln353Arg
ENST00000613082.1:n.453A>G
ENST00000614273.1:c.1058A>G ENSP00000483678.1:p.Gln353Arg
NM_000104.3:c.1058A>G NP_000095.2:p.Gln353Arg
NM_000104.4:c.1058A>G MANE Select NP_000095.2:p.Gln353Arg