Canonical Allele Identifier: CA346329488
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075066-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075066A>C , CM000664.2:g.38075066A>C GRCh38
NC_000002.11:g.38302209A>C , CM000664.1:g.38302209A>C GRCh37
NC_000002.10:g.38155713A>C NCBI36
NG_008386.2:g.6036T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.323T>G ENSP00000478839.2:p.Val108Gly
ENST00000610745.5:c.323T>G MANE Select ENSP00000478561.1:p.Val108Gly
ENST00000490576.1:c.323T>G ENSP00000478839.1:p.Val108Gly
ENST00000494864.1:c.-70-3756T>G ENSP00000479876.1:n.-70-3756T>G
ENST00000610745.4:c.323T>G ENSP00000478561.1:p.Val108Gly
ENST00000613082.1:n.376-658T>G
ENST00000614273.1:c.323T>G ENSP00000483678.1:p.Val108Gly
NM_000104.3:c.323T>G NP_000095.2:p.Val108Gly
NM_000104.4:c.323T>G MANE Select NP_000095.2:p.Val108Gly