Canonical Allele Identifier: CA346330069
Gene: CYP1B1 HGNC NCBI

Linked Data

gnomAD v4: 2-38075373-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075373T>G , CM000664.2:g.38075373T>G GRCh38
NC_000002.11:g.38302516T>G , CM000664.1:g.38302516T>G GRCh37
NC_000002.10:g.38156020T>G NCBI36
NG_008386.2:g.5729A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.16A>C ENSP00000478839.2:p.Ser6Arg
ENST00000610745.5:c.16A>C MANE Select ENSP00000478561.1:p.Ser6Arg
ENST00000490576.1:c.16A>C ENSP00000478839.1:p.Ser6Arg
ENST00000494864.1:c.-70-4063A>C ENSP00000479876.1:n.-70-4063A>C
ENST00000610745.4:c.16A>C ENSP00000478561.1:p.Ser6Arg
ENST00000613082.1:n.375+407A>C
ENST00000614273.1:c.16A>C ENSP00000483678.1:p.Ser6Arg
NM_000104.3:c.16A>C NP_000095.2:p.Ser6Arg
NM_000104.4:c.16A>C MANE Select NP_000095.2:p.Ser6Arg