Canonical Allele Identifier: CA145739
Gene: CYP1B1 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 92436
dbSNP Id: rs10012

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075247G>C , CM000664.2:g.38075247G>C GRCh38
NC_000002.11:g.38302390G>C , CM000664.1:g.38302390G>C GRCh37
NC_000002.10:g.38155894G>C NCBI36
NG_008386.2:g.5855C>G

Transcript Alleles

HGVS Amino-acid change
NM_000104.3:c.142C>G VV NP_000095.2:p.Arg48Gly
ENST00000490576.1:c.142C>G ENSP00000478839.1:p.Arg48Gly
ENST00000494864.1:c.-70-3937C>G ENSP00000479876.1:p.=
ENST00000610745.4:c.142C>G ENSP00000478561.1:p.Arg48Gly
ENST00000613082.1:n.375+533C>G
ENST00000614273.1:c.142C>G ENSP00000483678.1:p.Arg48Gly