Canonical Allele Identifier: CA425864349
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1267460834
gnomAD v2: 2-38298129-C-G
gnomAD v3: 2-38070986-C-G
gnomAD v4: 2-38070986-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38070986C>G , CM000664.2:g.38070986C>G GRCh38
NC_000002.11:g.38298129C>G , CM000664.1:g.38298129C>G GRCh37
NC_000002.10:g.38151633C>G NCBI36
NG_008386.2:g.10116G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1368G>C ENSP00000478839.2:p.Leu456=
ENST00000610745.5:c.1368G>C MANE Select ENSP00000478561.1:p.Leu456=
ENST00000494864.1:c.255G>C ENSP00000479876.1:p.Leu85=
ENST00000610745.4:c.1368G>C ENSP00000478561.1:p.Leu456=
ENST00000614273.1:c.1368G>C ENSP00000483678.1:p.Leu456=
NM_000104.3:c.1368G>C NP_000095.2:p.Leu456=
NM_000104.4:c.1368G>C MANE Select NP_000095.2:p.Leu456=