Canonical Allele Identifier: CA2658667742
Gene: CYP1B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38071276del , CM000664.2:g.38071276del GRCh38
NC_000002.11:g.38298419del , CM000664.1:g.38298419del GRCh37
NC_000002.10:g.38151923del NCBI36
NG_008386.2:g.9827del

Transcript Alleles

HGVS Amino-acid change
ENST00000490576.2:c.1079del ENSP00000478839.2:p.Leu360TrpfsTer?
ENST00000610745.5:c.1079del MANE Select ENSP00000478561.1:p.Leu360TrpfsTer?
ENST00000492443.1:n.457del
ENST00000494864.1:c.-35del ENSP00000479876.1:n.-35del
ENST00000610745.4:c.1079del ENSP00000478561.1:p.Leu360TrpfsTer?
ENST00000613082.1:n.474del
ENST00000614273.1:c.1079del ENSP00000483678.1:p.Leu360TrpfsTer?
NM_000104.3:c.1079del NP_000095.2:p.Leu360TrpfsTer?
NM_000104.4:c.1079del MANE Select NP_000095.2:p.Leu360TrpfsTer?