Canonical Allele Identifier: CA346329337
Gene: CYP1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1429075811
gnomAD v2: 2-38302134-G-A
gnomAD v4: 2-38074991-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38074991G>A , CM000664.2:g.38074991G>A GRCh38
NC_000002.11:g.38302134G>A , CM000664.1:g.38302134G>A GRCh37
NC_000002.10:g.38155638G>A NCBI36
NG_008386.2:g.6111C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.398C>T ENSP00000478839.2:p.Ala133Val
ENST00000610745.5:c.398C>T MANE Select ENSP00000478561.1:p.Ala133Val
ENST00000490576.1:c.398C>T ENSP00000478839.1:p.Ala133Val
ENST00000494864.1:c.-70-3681C>T ENSP00000479876.1:n.-70-3681C>T
ENST00000610745.4:c.398C>T ENSP00000478561.1:p.Ala133Val
ENST00000613082.1:n.376-583C>T
ENST00000614273.1:c.398C>T ENSP00000483678.1:p.Ala133Val
NM_000104.3:c.398C>T NP_000095.2:p.Ala133Val
NM_000104.4:c.398C>T MANE Select NP_000095.2:p.Ala133Val