Canonical Allele Identifier: CA1245626115
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071087T= , CM000664.2:g.38071087T= GRCh38
NC_000002.11:g.38298230T= , CM000664.1:g.38298230T= GRCh37
NC_000002.10:g.38151734T= NCBI36
NG_008386.2:g.10015A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.1267A= ENSP00000478839.2:p.Asn423=
ENST00000610745.5:c.1267A= MANE Select ENSP00000478561.1:p.Asn423=
ENST00000492443.1:n.645A=
ENST00000494864.1:c.154A= ENSP00000479876.1:p.Asn52=
ENST00000610745.4:c.1267A= ENSP00000478561.1:p.Asn423=
ENST00000614273.1:c.1267A= ENSP00000483678.1:p.Asn423=
NM_000104.3:c.1267A= NP_000095.2:p.Asn423=
NM_000104.4:c.1267A= MANE Select NP_000095.2:p.Asn423=